Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP272627.RAMqvI5aSGm7BIatXgr5De33lNEbBuA5adSWjBFE2m1vg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP272627.RAMqvI5aSGm7BIatXgr5De33lNEbBuA5adSWjBFE2m1vg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP272627.RAMqvI5aSGm7BIatXgr5De33lNEbBuA5adSWjBFE2m1vg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP272627.RAMqvI5aSGm7BIatXgr5De33lNEbBuA5adSWjBFE2m1vg130_provenance.
- NP272627.RAMqvI5aSGm7BIatXgr5De33lNEbBuA5adSWjBFE2m1vg130_assertion description "[We performed molecular analysis of BRAF in the largest cohort of ECD patients studied to date followed by N/KRAS, PIK3CA, and AKT1 mutational analysis in BRAF wild-type patients.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP272627.RAMqvI5aSGm7BIatXgr5De33lNEbBuA5adSWjBFE2m1vg130_provenance.
- NP272627.RAMqvI5aSGm7BIatXgr5De33lNEbBuA5adSWjBFE2m1vg130_assertion evidence source_evidence_literature NP272627.RAMqvI5aSGm7BIatXgr5De33lNEbBuA5adSWjBFE2m1vg130_provenance.
- NP272627.RAMqvI5aSGm7BIatXgr5De33lNEbBuA5adSWjBFE2m1vg130_assertion SIO_000772 25150293 NP272627.RAMqvI5aSGm7BIatXgr5De33lNEbBuA5adSWjBFE2m1vg130_provenance.
- NP272627.RAMqvI5aSGm7BIatXgr5De33lNEbBuA5adSWjBFE2m1vg130_assertion wasDerivedFrom befree-20150227 NP272627.RAMqvI5aSGm7BIatXgr5De33lNEbBuA5adSWjBFE2m1vg130_provenance.
- NP272627.RAMqvI5aSGm7BIatXgr5De33lNEbBuA5adSWjBFE2m1vg130_assertion wasGeneratedBy ECO_0000203 NP272627.RAMqvI5aSGm7BIatXgr5De33lNEbBuA5adSWjBFE2m1vg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP272627.RAMqvI5aSGm7BIatXgr5De33lNEbBuA5adSWjBFE2m1vg130_provenance.