Nanopublications LDF server

Matches in Nanopublications for { ?s ?p "[Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in the gene encoding for spatacsin at the SPG11 locus on chromosome 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ?g. }

• NP772742.RAcBlaKK7ReZS92f_a9NxvErthHyfrD3eMPGPWxGnsjf0130_assertion description "[Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in the gene encoding for spatacsin at the SPG11 locus on chromosome 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP772742.RAcBlaKK7ReZS92f_a9NxvErthHyfrD3eMPGPWxGnsjf0130_provenance.
• NP879741.RApPT-eNbHfZWxKpoSs4jfROjEVM1l4lZAradCnE05LUo130_assertion description "[Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in the gene encoding for spatacsin at the SPG11 locus on chromosome 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP879741.RApPT-eNbHfZWxKpoSs4jfROjEVM1l4lZAradCnE05LUo130_provenance.
• NP520172.RASO6du4fFNIQthem819IbwJ5oHBgGTT89t0DwutGQhCs130_assertion description "[Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in the gene encoding for spatacsin at the SPG11 locus on chromosome 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP520172.RASO6du4fFNIQthem819IbwJ5oHBgGTT89t0DwutGQhCs130_provenance.
• NP450812.RAIpxUtUMSEsazoQWb2J2gOFAl3cQL6n_AFiJD-4y3KUc130_assertion description "[Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in the gene encoding for spatacsin at the SPG11 locus on chromosome 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP450812.RAIpxUtUMSEsazoQWb2J2gOFAl3cQL6n_AFiJD-4y3KUc130_provenance.
• NP948434.RAA6xYimsGIbSxp8QF3qVJq_oRyrH5pg7zXdcmr58fzKs130_assertion description "[Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in the gene encoding for spatacsin at the SPG11 locus on chromosome 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948434.RAA6xYimsGIbSxp8QF3qVJq_oRyrH5pg7zXdcmr58fzKs130_provenance.
• NP783452.RAgnDd7hiR7pyemnSb_ygoKR0vymzcFVXBgrbmZUiI1jg130_assertion description "[Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in the gene encoding for spatacsin at the SPG11 locus on chromosome 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP783452.RAgnDd7hiR7pyemnSb_ygoKR0vymzcFVXBgrbmZUiI1jg130_provenance.
• NP661596.RANzcogjnqRl-SlKkeaQE7291P16fQfSBqWkL_jn6kkIY130_assertion description "[Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in the gene encoding for spatacsin at the SPG11 locus on chromosome 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP661596.RANzcogjnqRl-SlKkeaQE7291P16fQfSBqWkL_jn6kkIY130_provenance.
• NP948440.RA-vL_O0udwA2agi313qGVeBaeBHP25aTBHConl29BuH4130_assertion description "[Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in the gene encoding for spatacsin at the SPG11 locus on chromosome 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP948440.RA-vL_O0udwA2agi313qGVeBaeBHP25aTBHConl29BuH4130_provenance.
• NP721173.RA9PoCN_Pf2BN87wIxSsMGev2fwU_Bu5vwhvXrUdF9v1k130_assertion description "[Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in the gene encoding for spatacsin at the SPG11 locus on chromosome 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP721173.RA9PoCN_Pf2BN87wIxSsMGev2fwU_Bu5vwhvXrUdF9v1k130_provenance.
• NP721175.RALVzq4a51130EAiwMJFI0xD0yrLYVdKpI-ruzqRAIpVw130_assertion description "[Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in the gene encoding for spatacsin at the SPG11 locus on chromosome 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP721175.RALVzq4a51130EAiwMJFI0xD0yrLYVdKpI-ruzqRAIpVw130_provenance.
• assertion description "[Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in the gene encoding for spatacsin at the SPG11 locus on chromosome 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in the gene encoding for spatacsin at the SPG11 locus on chromosome 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in the gene encoding for spatacsin at the SPG11 locus on chromosome 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.
• assertion description "[Autosomal recessive hereditary spastic paraplegia (AR HSP) with thin corpus callosum (TCC) is a rare neurodegenerative disorder often caused by mutations in the gene encoding for spatacsin at the SPG11 locus on chromosome 15q.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." provenance.