Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP358298.RA54CDo80PylRXrSbZrNj3CvcGKW4hV7kyM5jJJ0FRkA0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP358298.RA54CDo80PylRXrSbZrNj3CvcGKW4hV7kyM5jJJ0FRkA0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP358298.RA54CDo80PylRXrSbZrNj3CvcGKW4hV7kyM5jJJ0FRkA0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP358298.RA54CDo80PylRXrSbZrNj3CvcGKW4hV7kyM5jJJ0FRkA0130_provenance.
- NP358298.RA54CDo80PylRXrSbZrNj3CvcGKW4hV7kyM5jJJ0FRkA0130_assertion description "[We found five mutations of the VHL gene and frequent LOH (50%) only in non-papillary clear cell RCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP358298.RA54CDo80PylRXrSbZrNj3CvcGKW4hV7kyM5jJJ0FRkA0130_provenance.
- NP358298.RA54CDo80PylRXrSbZrNj3CvcGKW4hV7kyM5jJJ0FRkA0130_assertion evidence source_evidence_literature NP358298.RA54CDo80PylRXrSbZrNj3CvcGKW4hV7kyM5jJJ0FRkA0130_provenance.
- NP358298.RA54CDo80PylRXrSbZrNj3CvcGKW4hV7kyM5jJJ0FRkA0130_assertion SIO_000772 12076276 NP358298.RA54CDo80PylRXrSbZrNj3CvcGKW4hV7kyM5jJJ0FRkA0130_provenance.
- NP358298.RA54CDo80PylRXrSbZrNj3CvcGKW4hV7kyM5jJJ0FRkA0130_assertion wasDerivedFrom befree-2016 NP358298.RA54CDo80PylRXrSbZrNj3CvcGKW4hV7kyM5jJJ0FRkA0130_provenance.
- NP358298.RA54CDo80PylRXrSbZrNj3CvcGKW4hV7kyM5jJJ0FRkA0130_assertion wasGeneratedBy ECO_0000203 NP358298.RA54CDo80PylRXrSbZrNj3CvcGKW4hV7kyM5jJJ0FRkA0130_provenance.
- befree-2016 importedOn "2016-02-19" NP358298.RA54CDo80PylRXrSbZrNj3CvcGKW4hV7kyM5jJJ0FRkA0130_provenance.