Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP625069.RA3CVLKVdfE3XpMCPvVFYxVTrL2rOb_3KfEmLqQ1PXBfQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP625069.RA3CVLKVdfE3XpMCPvVFYxVTrL2rOb_3KfEmLqQ1PXBfQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP625069.RA3CVLKVdfE3XpMCPvVFYxVTrL2rOb_3KfEmLqQ1PXBfQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP625069.RA3CVLKVdfE3XpMCPvVFYxVTrL2rOb_3KfEmLqQ1PXBfQ130_provenance.
- NP625069.RA3CVLKVdfE3XpMCPvVFYxVTrL2rOb_3KfEmLqQ1PXBfQ130_assertion description "[Our data indicate that BRAF gene mutations are relatively rare events in HNSCC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP625069.RA3CVLKVdfE3XpMCPvVFYxVTrL2rOb_3KfEmLqQ1PXBfQ130_provenance.
- NP625069.RA3CVLKVdfE3XpMCPvVFYxVTrL2rOb_3KfEmLqQ1PXBfQ130_assertion evidence source_evidence_literature NP625069.RA3CVLKVdfE3XpMCPvVFYxVTrL2rOb_3KfEmLqQ1PXBfQ130_provenance.
- NP625069.RA3CVLKVdfE3XpMCPvVFYxVTrL2rOb_3KfEmLqQ1PXBfQ130_assertion SIO_000772 12879021 NP625069.RA3CVLKVdfE3XpMCPvVFYxVTrL2rOb_3KfEmLqQ1PXBfQ130_provenance.
- NP625069.RA3CVLKVdfE3XpMCPvVFYxVTrL2rOb_3KfEmLqQ1PXBfQ130_assertion wasDerivedFrom befree-20140225 NP625069.RA3CVLKVdfE3XpMCPvVFYxVTrL2rOb_3KfEmLqQ1PXBfQ130_provenance.
- NP625069.RA3CVLKVdfE3XpMCPvVFYxVTrL2rOb_3KfEmLqQ1PXBfQ130_assertion wasGeneratedBy ECO_0000203 NP625069.RA3CVLKVdfE3XpMCPvVFYxVTrL2rOb_3KfEmLqQ1PXBfQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP625069.RA3CVLKVdfE3XpMCPvVFYxVTrL2rOb_3KfEmLqQ1PXBfQ130_provenance.