Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP631779.RAguRkImwlhB0ywfIzTYlO50m-8yfhnqs5rt4lGXvs0Gw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP631779.RAguRkImwlhB0ywfIzTYlO50m-8yfhnqs5rt4lGXvs0Gw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP631779.RAguRkImwlhB0ywfIzTYlO50m-8yfhnqs5rt4lGXvs0Gw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP631779.RAguRkImwlhB0ywfIzTYlO50m-8yfhnqs5rt4lGXvs0Gw130_provenance.
- NP631779.RAguRkImwlhB0ywfIzTYlO50m-8yfhnqs5rt4lGXvs0Gw130_assertion description "[The aim of our research was to assess the frequency of NBS1 mutations in patients with larynx cancer only (LC) and with MPT.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP631779.RAguRkImwlhB0ywfIzTYlO50m-8yfhnqs5rt4lGXvs0Gw130_provenance.
- NP631779.RAguRkImwlhB0ywfIzTYlO50m-8yfhnqs5rt4lGXvs0Gw130_assertion evidence source_evidence_literature NP631779.RAguRkImwlhB0ywfIzTYlO50m-8yfhnqs5rt4lGXvs0Gw130_provenance.
- NP631779.RAguRkImwlhB0ywfIzTYlO50m-8yfhnqs5rt4lGXvs0Gw130_assertion SIO_000772 17894553 NP631779.RAguRkImwlhB0ywfIzTYlO50m-8yfhnqs5rt4lGXvs0Gw130_provenance.
- NP631779.RAguRkImwlhB0ywfIzTYlO50m-8yfhnqs5rt4lGXvs0Gw130_assertion wasDerivedFrom befree-2016 NP631779.RAguRkImwlhB0ywfIzTYlO50m-8yfhnqs5rt4lGXvs0Gw130_provenance.
- NP631779.RAguRkImwlhB0ywfIzTYlO50m-8yfhnqs5rt4lGXvs0Gw130_assertion wasGeneratedBy ECO_0000203 NP631779.RAguRkImwlhB0ywfIzTYlO50m-8yfhnqs5rt4lGXvs0Gw130_provenance.
- befree-2016 importedOn "2016-02-19" NP631779.RAguRkImwlhB0ywfIzTYlO50m-8yfhnqs5rt4lGXvs0Gw130_provenance.