Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP173540.RA4Dmdh5_BiQ5qml5nuD9fBcKh3EfmNssF2Zc7Y1g_UrY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP173540.RA4Dmdh5_BiQ5qml5nuD9fBcKh3EfmNssF2Zc7Y1g_UrY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP173540.RA4Dmdh5_BiQ5qml5nuD9fBcKh3EfmNssF2Zc7Y1g_UrY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP173540.RA4Dmdh5_BiQ5qml5nuD9fBcKh3EfmNssF2Zc7Y1g_UrY130_provenance.
- NP173540.RA4Dmdh5_BiQ5qml5nuD9fBcKh3EfmNssF2Zc7Y1g_UrY130_assertion description "[Recently, a 342-kb deletion involving GJB6 was associated with autosomal-recessive non-syndromic hearing loss (NSHL) and in combination with a GJB2 mutation with digenic NSHL.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP173540.RA4Dmdh5_BiQ5qml5nuD9fBcKh3EfmNssF2Zc7Y1g_UrY130_provenance.
- NP173540.RA4Dmdh5_BiQ5qml5nuD9fBcKh3EfmNssF2Zc7Y1g_UrY130_assertion evidence source_evidence_literature NP173540.RA4Dmdh5_BiQ5qml5nuD9fBcKh3EfmNssF2Zc7Y1g_UrY130_provenance.
- NP173540.RA4Dmdh5_BiQ5qml5nuD9fBcKh3EfmNssF2Zc7Y1g_UrY130_assertion SIO_000772 12872268 NP173540.RA4Dmdh5_BiQ5qml5nuD9fBcKh3EfmNssF2Zc7Y1g_UrY130_provenance.
- NP173540.RA4Dmdh5_BiQ5qml5nuD9fBcKh3EfmNssF2Zc7Y1g_UrY130_assertion wasDerivedFrom befree-20140225 NP173540.RA4Dmdh5_BiQ5qml5nuD9fBcKh3EfmNssF2Zc7Y1g_UrY130_provenance.
- NP173540.RA4Dmdh5_BiQ5qml5nuD9fBcKh3EfmNssF2Zc7Y1g_UrY130_assertion wasGeneratedBy ECO_0000203 NP173540.RA4Dmdh5_BiQ5qml5nuD9fBcKh3EfmNssF2Zc7Y1g_UrY130_provenance.
- befree-20140225 importedOn "2014-02-25" NP173540.RA4Dmdh5_BiQ5qml5nuD9fBcKh3EfmNssF2Zc7Y1g_UrY130_provenance.