Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP479388.RAHPmPhpQoRay1DwZyYJ96cojS7cgzUPLbUa0rYRh39AM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP479388.RAHPmPhpQoRay1DwZyYJ96cojS7cgzUPLbUa0rYRh39AM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP479388.RAHPmPhpQoRay1DwZyYJ96cojS7cgzUPLbUa0rYRh39AM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP479388.RAHPmPhpQoRay1DwZyYJ96cojS7cgzUPLbUa0rYRh39AM130_provenance.
- NP479388.RAHPmPhpQoRay1DwZyYJ96cojS7cgzUPLbUa0rYRh39AM130_assertion description "[Mutations in the Usher syndrome type I causing genes are also recorded in non-syndromic hearing loss cases and mutations in USH2A in non-syndromic retinitis pigmentosa.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP479388.RAHPmPhpQoRay1DwZyYJ96cojS7cgzUPLbUa0rYRh39AM130_provenance.
- NP479388.RAHPmPhpQoRay1DwZyYJ96cojS7cgzUPLbUa0rYRh39AM130_assertion evidence source_evidence_literature NP479388.RAHPmPhpQoRay1DwZyYJ96cojS7cgzUPLbUa0rYRh39AM130_provenance.
- NP479388.RAHPmPhpQoRay1DwZyYJ96cojS7cgzUPLbUa0rYRh39AM130_assertion SIO_000772 18484607 NP479388.RAHPmPhpQoRay1DwZyYJ96cojS7cgzUPLbUa0rYRh39AM130_provenance.
- NP479388.RAHPmPhpQoRay1DwZyYJ96cojS7cgzUPLbUa0rYRh39AM130_assertion wasDerivedFrom befree-20140225 NP479388.RAHPmPhpQoRay1DwZyYJ96cojS7cgzUPLbUa0rYRh39AM130_provenance.
- NP479388.RAHPmPhpQoRay1DwZyYJ96cojS7cgzUPLbUa0rYRh39AM130_assertion wasGeneratedBy ECO_0000203 NP479388.RAHPmPhpQoRay1DwZyYJ96cojS7cgzUPLbUa0rYRh39AM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP479388.RAHPmPhpQoRay1DwZyYJ96cojS7cgzUPLbUa0rYRh39AM130_provenance.