Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1077722.RAzV-NBNqqtAPo8ya00imMOa5VEl90XcGJyDGmxTD7veo130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1077722.RAzV-NBNqqtAPo8ya00imMOa5VEl90XcGJyDGmxTD7veo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1077722.RAzV-NBNqqtAPo8ya00imMOa5VEl90XcGJyDGmxTD7veo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1077722.RAzV-NBNqqtAPo8ya00imMOa5VEl90XcGJyDGmxTD7veo130_provenance.
- NP1077722.RAzV-NBNqqtAPo8ya00imMOa5VEl90XcGJyDGmxTD7veo130_assertion description "[Although it has recently been shown that ?97�% of all adult GCT harbor a novel somatic missense mutation in the FOXL2 gene, given its almost universal presence, it does not explain differences in tumor stage and/or recurrence.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1077722.RAzV-NBNqqtAPo8ya00imMOa5VEl90XcGJyDGmxTD7veo130_provenance.
- NP1077722.RAzV-NBNqqtAPo8ya00imMOa5VEl90XcGJyDGmxTD7veo130_assertion evidence source_evidence_literature NP1077722.RAzV-NBNqqtAPo8ya00imMOa5VEl90XcGJyDGmxTD7veo130_provenance.
- NP1077722.RAzV-NBNqqtAPo8ya00imMOa5VEl90XcGJyDGmxTD7veo130_assertion SIO_000772 23674259 NP1077722.RAzV-NBNqqtAPo8ya00imMOa5VEl90XcGJyDGmxTD7veo130_provenance.
- NP1077722.RAzV-NBNqqtAPo8ya00imMOa5VEl90XcGJyDGmxTD7veo130_assertion wasDerivedFrom befree-2016 NP1077722.RAzV-NBNqqtAPo8ya00imMOa5VEl90XcGJyDGmxTD7veo130_provenance.
- NP1077722.RAzV-NBNqqtAPo8ya00imMOa5VEl90XcGJyDGmxTD7veo130_assertion wasGeneratedBy ECO_0000203 NP1077722.RAzV-NBNqqtAPo8ya00imMOa5VEl90XcGJyDGmxTD7veo130_provenance.
- befree-2016 importedOn "2016-02-19" NP1077722.RAzV-NBNqqtAPo8ya00imMOa5VEl90XcGJyDGmxTD7veo130_provenance.