Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_provenance.
- 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.
- befree-2016 importedOn "2016-02-19" NP919546.RAnh6clfTr0zja0pPwJz5v88Mn3xrBF43ez2s-BXA_xIE130_provenance.