Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1095869.RAhmMPu7om675g16PyALHC8FLVEwjJrkbUI1fgQ87Mx64130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1095869.RAhmMPu7om675g16PyALHC8FLVEwjJrkbUI1fgQ87Mx64130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1095869.RAhmMPu7om675g16PyALHC8FLVEwjJrkbUI1fgQ87Mx64130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1095869.RAhmMPu7om675g16PyALHC8FLVEwjJrkbUI1fgQ87Mx64130_provenance.
- NP1095869.RAhmMPu7om675g16PyALHC8FLVEwjJrkbUI1fgQ87Mx64130_assertion description "[KRAS mutations (41%) predominated in CRC, followed by loss of PTEN expression (16%), PIK3CA (5%) and BRAF (5%) mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1095869.RAhmMPu7om675g16PyALHC8FLVEwjJrkbUI1fgQ87Mx64130_provenance.
- NP1095869.RAhmMPu7om675g16PyALHC8FLVEwjJrkbUI1fgQ87Mx64130_assertion evidence source_evidence_literature NP1095869.RAhmMPu7om675g16PyALHC8FLVEwjJrkbUI1fgQ87Mx64130_provenance.
- NP1095869.RAhmMPu7om675g16PyALHC8FLVEwjJrkbUI1fgQ87Mx64130_assertion SIO_000772 23876834 NP1095869.RAhmMPu7om675g16PyALHC8FLVEwjJrkbUI1fgQ87Mx64130_provenance.
- NP1095869.RAhmMPu7om675g16PyALHC8FLVEwjJrkbUI1fgQ87Mx64130_assertion wasDerivedFrom befree-2016 NP1095869.RAhmMPu7om675g16PyALHC8FLVEwjJrkbUI1fgQ87Mx64130_provenance.
- NP1095869.RAhmMPu7om675g16PyALHC8FLVEwjJrkbUI1fgQ87Mx64130_assertion wasGeneratedBy ECO_0000203 NP1095869.RAhmMPu7om675g16PyALHC8FLVEwjJrkbUI1fgQ87Mx64130_provenance.
- befree-2016 importedOn "2016-02-19" NP1095869.RAhmMPu7om675g16PyALHC8FLVEwjJrkbUI1fgQ87Mx64130_provenance.