Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP284036.RAcETkKhDor2fi9gKQdLbnA7_9nuQK3ckEWbzbYYldXxA130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP284036.RAcETkKhDor2fi9gKQdLbnA7_9nuQK3ckEWbzbYYldXxA130_provenance.
• NP302754.RAB-PZx2SSN8RjEwLeyMc8cLh5FB1yZQz-TCC9iKOTLLo130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP302754.RAB-PZx2SSN8RjEwLeyMc8cLh5FB1yZQz-TCC9iKOTLLo130_provenance.
• NP548171.RADRMfIOUd377L_bJHZYq3s2c5WTbuz-AZNv6_d2BSwgc130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP548171.RADRMfIOUd377L_bJHZYq3s2c5WTbuz-AZNv6_d2BSwgc130_provenance.
• NP256678.RAW6DktXDj7tsM7QrdM1VAJFqBm6qSJBztAsLgCqQnZVQ130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP256678.RAW6DktXDj7tsM7QrdM1VAJFqBm6qSJBztAsLgCqQnZVQ130_provenance.
• NP767240.RAmVGtm7flLQ7pCm3e4jpyCyE7j0ZBftD4pKxUeE0QxUE130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP767240.RAmVGtm7flLQ7pCm3e4jpyCyE7j0ZBftD4pKxUeE0QxUE130_provenance.
• NP518783.RAapMfvs7d4PucMsnWT4dcpAfCkFGaN6GDlwVP7iXZXi4130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP518783.RAapMfvs7d4PucMsnWT4dcpAfCkFGaN6GDlwVP7iXZXi4130_provenance.
• NP401772.RAEft9oAZdBXYpAbJD-HPxAhktaqnJT5asmrxIlxSCPKM130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401772.RAEft9oAZdBXYpAbJD-HPxAhktaqnJT5asmrxIlxSCPKM130_provenance.
• NP438330.RAJvApbQWWOBm78ceTOZJMw1RrFEZk6H6aAaIppmW-Z_U130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP438330.RAJvApbQWWOBm78ceTOZJMw1RrFEZk6H6aAaIppmW-Z_U130_provenance.
• NP520234.RA1H-tl1mODifUMsCirDlh12cdtMM0FQu9Umn8oRqaXNY130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP520234.RA1H-tl1mODifUMsCirDlh12cdtMM0FQu9Umn8oRqaXNY130_provenance.
• NP239552.RAxK_vDuCZP670d32w0MMUMrhAL8w1yssE5yUEV83miM0130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP239552.RAxK_vDuCZP670d32w0MMUMrhAL8w1yssE5yUEV83miM0130_provenance.
• NP416899.RAw5wdSx1-lFbpp_3uUsp2vH6BMY924cbtrhqlyJnv7bs130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP416899.RAw5wdSx1-lFbpp_3uUsp2vH6BMY924cbtrhqlyJnv7bs130_provenance.
• NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP869311.RAPLlxBe--mZ9DisouDtpw-ccYq-U6SXfRdquEn77HTmE130_provenance.
• NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783086.RA8a6lPg3UVWE2ZqVU6USoJMRGjuBXYIPGs2yfEPAL1d8130_provenance.
• NP859449.RAYQ_c8_mIIFYcEx8j84l8jnQko3jKn8lSWCPxYe6-zPw130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP859449.RAYQ_c8_mIIFYcEx8j84l8jnQko3jKn8lSWCPxYe6-zPw130_provenance.
• NP859447.RAwuwzuWMKVPPyKeqNN8cIVSgxAqlhXpc8mZbEgS2ee_0130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP859447.RAwuwzuWMKVPPyKeqNN8cIVSgxAqlhXpc8mZbEgS2ee_0130_provenance.
• NP1396574.RAwmWPIu6PttLI_qiNvtGseU2rGhKQ8WmvG65rh6YTFrA130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1396574.RAwmWPIu6PttLI_qiNvtGseU2rGhKQ8WmvG65rh6YTFrA130_provenance.
• NP1396569.RASsiy8pYIR0wOdHtTe_HJ8NAU_HntmHKz9Plxb1u57lg130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1396569.RASsiy8pYIR0wOdHtTe_HJ8NAU_HntmHKz9Plxb1u57lg130_provenance.
• NP1396571.RAQs70WC-MbPyx_9F8g0OKylK_XDmhR70EQADjWtk-VIU130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1396571.RAQs70WC-MbPyx_9F8g0OKylK_XDmhR70EQADjWtk-VIU130_provenance.
• NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1396570.RAJITLHObyoLW6tkY0BcXAFw5ehzjqOu4xHgsAcZ7Cd2U130_provenance.
• NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP859434.RAkYmeexCmnTBh6Iw91x3NNVnd0lRZT_IlzHyAx_IIX4c130_provenance.
• NP783095.RAq1keQEmgiKbeDbb6kvbzv08j54fNrubbKnUsk92kYrs130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783095.RAq1keQEmgiKbeDbb6kvbzv08j54fNrubbKnUsk92kYrs130_provenance.
• NP1396572.RAgZpzGMQ2Shufa-u9nhe0A7WQ6EuZ_uRzzv48iadFeJo130_assertion description "[ZNF179, a RING finger protein encoding gene, has been mapped within the critical deletion region for Smith-Magenis syndrome (SMS), a disorder characterized by mental retardation and multiple congenital anomalies associated with del(17)(p11.2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1396572.RAgZpzGMQ2Shufa-u9nhe0A7WQ6EuZ_uRzzv48iadFeJo130_provenance.