Matches in Nanopublications for { ?s ?p "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }
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- NP302639.RAVZLevVA3-NF3QZ_-Kc4IUjic7g9TB4U5pm7KttCPnuw130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP302639.RAVZLevVA3-NF3QZ_-Kc4IUjic7g9TB4U5pm7KttCPnuw130_provenance.
- NP665116.RAQYvhow0_euJ5jYoO1Lfx2UnknIJH2BDHet0wrNt1xhw130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP665116.RAQYvhow0_euJ5jYoO1Lfx2UnknIJH2BDHet0wrNt1xhw130_provenance.
- NP932067.RAaId0Aw-jndcgFq1ZCpe_ze0Rn_wQmStZvP84ltXLZr0130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP932067.RAaId0Aw-jndcgFq1ZCpe_ze0Rn_wQmStZvP84ltXLZr0130_provenance.
- NP516137.RAYtZZCWoVOt5i7igxL--3lBLax_3KGl7uxugL1f88Uhw130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP516137.RAYtZZCWoVOt5i7igxL--3lBLax_3KGl7uxugL1f88Uhw130_provenance.
- NP808099.RAium_RynkqWU2pjK0Bt8z7RFLb0w6-tgXuSSlyZqv-Ho130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP808099.RAium_RynkqWU2pjK0Bt8z7RFLb0w6-tgXuSSlyZqv-Ho130_provenance.
- NP893705.RAAWjjoE2di0IWXUmw8_t5dTtyItLZTdRPeyPRk5GtLuw130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP893705.RAAWjjoE2di0IWXUmw8_t5dTtyItLZTdRPeyPRk5GtLuw130_provenance.
- NP313738.RAxpSBL2KFi6KuUn2BuRGEgwliMbMQEATD7w7t4bZWPyU130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP313738.RAxpSBL2KFi6KuUn2BuRGEgwliMbMQEATD7w7t4bZWPyU130_provenance.
- NP404424.RAVGTNvRdsdZ-Qun0Lj5vCsDw1adMPbJMWGP6q_QdB_cw130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404424.RAVGTNvRdsdZ-Qun0Lj5vCsDw1adMPbJMWGP6q_QdB_cw130_provenance.
- NP404369.RA7_g5u8xY7F9rlm8zIvbF5CmkuQ2pnec9lzSAylNDgKs130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404369.RA7_g5u8xY7F9rlm8zIvbF5CmkuQ2pnec9lzSAylNDgKs130_provenance.
- NP893721.RATvKNtjJcwvFX2Dm_TjGDZ_yyI88Y9VoDmvDZxTYzN9M130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP893721.RATvKNtjJcwvFX2Dm_TjGDZ_yyI88Y9VoDmvDZxTYzN9M130_provenance.
- assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP1045490.RAW0ixfn50gustmWAfrIfmXADwf4ZeEjUiNjVTrVvC6do130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045490.RAW0ixfn50gustmWAfrIfmXADwf4ZeEjUiNjVTrVvC6do130_provenance.
- NP1045492.RAX5k5XJAL2MpvzJJrX5oXsBBFEDrYj6vle9VJGQ3H8oA130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045492.RAX5k5XJAL2MpvzJJrX5oXsBBFEDrYj6vle9VJGQ3H8oA130_provenance.
- assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
- NP404383.RAi21b7oCLWPHuS194hkMmDRi1Q29tQiJ3j1tHY73tPGk130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404383.RAi21b7oCLWPHuS194hkMmDRi1Q29tQiJ3j1tHY73tPGk130_provenance.
- NP404433.RAmg2sNI9ewIiefIkl9P-yk8T7iIFbPrDh60NIErPek4w130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP404433.RAmg2sNI9ewIiefIkl9P-yk8T7iIFbPrDh60NIErPek4w130_provenance.
- NP893710.RAF-u_mZgoypjnoeGnlhTZmJFN1k4TtDYtrRw4l1vEDAk130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP893710.RAF-u_mZgoypjnoeGnlhTZmJFN1k4TtDYtrRw4l1vEDAk130_provenance.
- NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP893724.RAOhW51A0bE6V9jsSY2B1vCs79tPn4b2noBcvopSpMK0A130_provenance.
- NP1045478.RAIm45mTyFT-dsQwWsXZi1q_9c4H68MD4M_c9vakqkFdg130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045478.RAIm45mTyFT-dsQwWsXZi1q_9c4H68MD4M_c9vakqkFdg130_provenance.
- NP1045479.RAMtw5WSliqTsaJdopjsAkphNreEVg5jyR40SroNo6QZM130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045479.RAMtw5WSliqTsaJdopjsAkphNreEVg5jyR40SroNo6QZM130_provenance.
- NP1045480.RAG4wNJUM6CmExe__nBu-sPqOxqWJFWhWIxWuzp4c-dzs130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045480.RAG4wNJUM6CmExe__nBu-sPqOxqWJFWhWIxWuzp4c-dzs130_provenance.
- NP1045487.RAK4AwFst9pE5rBribp14tryYxzIlenbc1v_Vq3APavyI130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045487.RAK4AwFst9pE5rBribp14tryYxzIlenbc1v_Vq3APavyI130_provenance.
- NP1045481.RAsBkhlKw0QWnY7qMx0tl_qE1UaTSv4tDUfjUiAkUZbRg130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045481.RAsBkhlKw0QWnY7qMx0tl_qE1UaTSv4tDUfjUiAkUZbRg130_provenance.
- NP1045483.RAs-JJtkATj2KiNBOFNjzHtdprryurTcZGSRjng72742A130_assertion description "[Contiguous gene deletions involving ANKRD11 in 16q24.3 are associated with autism spectrum disorder (ASD) and intellectual disability (ID), while 16q24.1 deletions affecting FOXF1 are associated with congenital renal malformations, alveolar capillary dysplasia, and various other abnormalities.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1045483.RAs-JJtkATj2KiNBOFNjzHtdprryurTcZGSRjng72742A130_provenance.