Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_assertion> ?p ?o ?g. }
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- NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_assertion type Assertion NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_head.
- NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_assertion description "[Mutations in GJB1, the gene for connexin 32 (Cx32) cause the second most common form of Charcot-Marie-Tooth disease (CMT1X).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_provenance.
- NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_assertion evidence source_evidence_literature NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_provenance.
- NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_assertion SIO_000772 21871435 NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_provenance.
- NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_assertion wasDerivedFrom befree-2016 NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_provenance.
- NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_assertion wasGeneratedBy ECO_0000203 NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_provenance.