Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP221948.RAOUPFDxTvU9427kFIYfJSGoO7GfZPq5b1aNlhXe0tHcI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP221948.RAOUPFDxTvU9427kFIYfJSGoO7GfZPq5b1aNlhXe0tHcI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP221948.RAOUPFDxTvU9427kFIYfJSGoO7GfZPq5b1aNlhXe0tHcI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP221948.RAOUPFDxTvU9427kFIYfJSGoO7GfZPq5b1aNlhXe0tHcI130_provenance.
- NP221948.RAOUPFDxTvU9427kFIYfJSGoO7GfZPq5b1aNlhXe0tHcI130_assertion description "[Six point mutations in non-muscle gamma-actin at the DFNA20/26 locus cause autosomal dominant nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP221948.RAOUPFDxTvU9427kFIYfJSGoO7GfZPq5b1aNlhXe0tHcI130_provenance.
- NP221948.RAOUPFDxTvU9427kFIYfJSGoO7GfZPq5b1aNlhXe0tHcI130_assertion evidence source_evidence_literature NP221948.RAOUPFDxTvU9427kFIYfJSGoO7GfZPq5b1aNlhXe0tHcI130_provenance.
- NP221948.RAOUPFDxTvU9427kFIYfJSGoO7GfZPq5b1aNlhXe0tHcI130_assertion SIO_000772 16690605 NP221948.RAOUPFDxTvU9427kFIYfJSGoO7GfZPq5b1aNlhXe0tHcI130_provenance.
- NP221948.RAOUPFDxTvU9427kFIYfJSGoO7GfZPq5b1aNlhXe0tHcI130_assertion wasDerivedFrom befree-20150227 NP221948.RAOUPFDxTvU9427kFIYfJSGoO7GfZPq5b1aNlhXe0tHcI130_provenance.
- NP221948.RAOUPFDxTvU9427kFIYfJSGoO7GfZPq5b1aNlhXe0tHcI130_assertion wasGeneratedBy ECO_0000203 NP221948.RAOUPFDxTvU9427kFIYfJSGoO7GfZPq5b1aNlhXe0tHcI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP221948.RAOUPFDxTvU9427kFIYfJSGoO7GfZPq5b1aNlhXe0tHcI130_provenance.