Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP353190.RAV0Y0-Rgq6wddznv-CbdDLbHk6XJ_MX1vLtaVVGIr0_Y130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP353190.RAV0Y0-Rgq6wddznv-CbdDLbHk6XJ_MX1vLtaVVGIr0_Y130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP353190.RAV0Y0-Rgq6wddznv-CbdDLbHk6XJ_MX1vLtaVVGIr0_Y130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP353190.RAV0Y0-Rgq6wddznv-CbdDLbHk6XJ_MX1vLtaVVGIr0_Y130_provenance.
- NP353190.RAV0Y0-Rgq6wddznv-CbdDLbHk6XJ_MX1vLtaVVGIr0_Y130_assertion description "[The high-level expression and stability of cochlin in the inner ear, even in the absence and severe atrophy of the fibrocytes that normally express COCH, are shown through these studies and further elucidate the pathobiologic events occurring in DFNA9 leading to hearing loss and vestibular dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP353190.RAV0Y0-Rgq6wddznv-CbdDLbHk6XJ_MX1vLtaVVGIr0_Y130_provenance.
- NP353190.RAV0Y0-Rgq6wddznv-CbdDLbHk6XJ_MX1vLtaVVGIr0_Y130_assertion evidence source_evidence_literature NP353190.RAV0Y0-Rgq6wddznv-CbdDLbHk6XJ_MX1vLtaVVGIr0_Y130_provenance.
- NP353190.RAV0Y0-Rgq6wddznv-CbdDLbHk6XJ_MX1vLtaVVGIr0_Y130_assertion SIO_000772 16481359 NP353190.RAV0Y0-Rgq6wddznv-CbdDLbHk6XJ_MX1vLtaVVGIr0_Y130_provenance.
- NP353190.RAV0Y0-Rgq6wddznv-CbdDLbHk6XJ_MX1vLtaVVGIr0_Y130_assertion wasDerivedFrom befree-20150227 NP353190.RAV0Y0-Rgq6wddznv-CbdDLbHk6XJ_MX1vLtaVVGIr0_Y130_provenance.
- NP353190.RAV0Y0-Rgq6wddznv-CbdDLbHk6XJ_MX1vLtaVVGIr0_Y130_assertion wasGeneratedBy ECO_0000203 NP353190.RAV0Y0-Rgq6wddznv-CbdDLbHk6XJ_MX1vLtaVVGIr0_Y130_provenance.
- befree-20150227 importedOn "2015-02-27" NP353190.RAV0Y0-Rgq6wddznv-CbdDLbHk6XJ_MX1vLtaVVGIr0_Y130_provenance.