Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1158176.RAW_XIqNK7txljCGwcTFoFNca-j21b2GYBk9Hiw_CHgj8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1158176.RAW_XIqNK7txljCGwcTFoFNca-j21b2GYBk9Hiw_CHgj8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1158176.RAW_XIqNK7txljCGwcTFoFNca-j21b2GYBk9Hiw_CHgj8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1158176.RAW_XIqNK7txljCGwcTFoFNca-j21b2GYBk9Hiw_CHgj8130_provenance.
- NP1158176.RAW_XIqNK7txljCGwcTFoFNca-j21b2GYBk9Hiw_CHgj8130_assertion description "[BRAF((V600E)) mutations were found in 14.3% of SSAs and 7.1% of RHPs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1158176.RAW_XIqNK7txljCGwcTFoFNca-j21b2GYBk9Hiw_CHgj8130_provenance.
- NP1158176.RAW_XIqNK7txljCGwcTFoFNca-j21b2GYBk9Hiw_CHgj8130_assertion evidence source_evidence_literature NP1158176.RAW_XIqNK7txljCGwcTFoFNca-j21b2GYBk9Hiw_CHgj8130_provenance.
- NP1158176.RAW_XIqNK7txljCGwcTFoFNca-j21b2GYBk9Hiw_CHgj8130_assertion SIO_000772 24570042 NP1158176.RAW_XIqNK7txljCGwcTFoFNca-j21b2GYBk9Hiw_CHgj8130_provenance.
- NP1158176.RAW_XIqNK7txljCGwcTFoFNca-j21b2GYBk9Hiw_CHgj8130_assertion wasDerivedFrom befree-2016 NP1158176.RAW_XIqNK7txljCGwcTFoFNca-j21b2GYBk9Hiw_CHgj8130_provenance.
- NP1158176.RAW_XIqNK7txljCGwcTFoFNca-j21b2GYBk9Hiw_CHgj8130_assertion wasGeneratedBy ECO_0000203 NP1158176.RAW_XIqNK7txljCGwcTFoFNca-j21b2GYBk9Hiw_CHgj8130_provenance.
- befree-2016 importedOn "2016-02-19" NP1158176.RAW_XIqNK7txljCGwcTFoFNca-j21b2GYBk9Hiw_CHgj8130_provenance.