Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP106341.RAhxZO0lCUl64qTajn8QtjhriaH0iBuS-4DD1jAeDNSVU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP106341.RAhxZO0lCUl64qTajn8QtjhriaH0iBuS-4DD1jAeDNSVU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP106341.RAhxZO0lCUl64qTajn8QtjhriaH0iBuS-4DD1jAeDNSVU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP106341.RAhxZO0lCUl64qTajn8QtjhriaH0iBuS-4DD1jAeDNSVU130_provenance.
- NP106341.RAhxZO0lCUl64qTajn8QtjhriaH0iBuS-4DD1jAeDNSVU130_assertion description "[GJB2 mutations in Iranians with autosomal recessive non-syndromic sensorineural hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP106341.RAhxZO0lCUl64qTajn8QtjhriaH0iBuS-4DD1jAeDNSVU130_provenance.
- NP106341.RAhxZO0lCUl64qTajn8QtjhriaH0iBuS-4DD1jAeDNSVU130_assertion evidence source_evidence_literature NP106341.RAhxZO0lCUl64qTajn8QtjhriaH0iBuS-4DD1jAeDNSVU130_provenance.
- NP106341.RAhxZO0lCUl64qTajn8QtjhriaH0iBuS-4DD1jAeDNSVU130_assertion SIO_000772 11968091 NP106341.RAhxZO0lCUl64qTajn8QtjhriaH0iBuS-4DD1jAeDNSVU130_provenance.
- NP106341.RAhxZO0lCUl64qTajn8QtjhriaH0iBuS-4DD1jAeDNSVU130_assertion wasDerivedFrom gad-20150221 NP106341.RAhxZO0lCUl64qTajn8QtjhriaH0iBuS-4DD1jAeDNSVU130_provenance.
- NP106341.RAhxZO0lCUl64qTajn8QtjhriaH0iBuS-4DD1jAeDNSVU130_assertion wasGeneratedBy ECO_0000203 NP106341.RAhxZO0lCUl64qTajn8QtjhriaH0iBuS-4DD1jAeDNSVU130_provenance.
- gad-20150221 importedOn "2015-02-21" NP106341.RAhxZO0lCUl64qTajn8QtjhriaH0iBuS-4DD1jAeDNSVU130_provenance.