Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP663039.RALCTmfLwE1rGl2-pj8r-lEMDtR1KY38UwVwW6LCt8AcY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP663039.RALCTmfLwE1rGl2-pj8r-lEMDtR1KY38UwVwW6LCt8AcY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP663039.RALCTmfLwE1rGl2-pj8r-lEMDtR1KY38UwVwW6LCt8AcY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP663039.RALCTmfLwE1rGl2-pj8r-lEMDtR1KY38UwVwW6LCt8AcY130_provenance.
- NP663039.RALCTmfLwE1rGl2-pj8r-lEMDtR1KY38UwVwW6LCt8AcY130_assertion description "[Exome sequencing identifies recurrent somatic RAC1 mutations in melanoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP663039.RALCTmfLwE1rGl2-pj8r-lEMDtR1KY38UwVwW6LCt8AcY130_provenance.
- NP663039.RALCTmfLwE1rGl2-pj8r-lEMDtR1KY38UwVwW6LCt8AcY130_assertion evidence source_evidence_literature NP663039.RALCTmfLwE1rGl2-pj8r-lEMDtR1KY38UwVwW6LCt8AcY130_provenance.
- NP663039.RALCTmfLwE1rGl2-pj8r-lEMDtR1KY38UwVwW6LCt8AcY130_assertion SIO_000772 22842228 NP663039.RALCTmfLwE1rGl2-pj8r-lEMDtR1KY38UwVwW6LCt8AcY130_provenance.
- NP663039.RALCTmfLwE1rGl2-pj8r-lEMDtR1KY38UwVwW6LCt8AcY130_assertion wasDerivedFrom befree-20150227 NP663039.RALCTmfLwE1rGl2-pj8r-lEMDtR1KY38UwVwW6LCt8AcY130_provenance.
- NP663039.RALCTmfLwE1rGl2-pj8r-lEMDtR1KY38UwVwW6LCt8AcY130_assertion wasGeneratedBy ECO_0000203 NP663039.RALCTmfLwE1rGl2-pj8r-lEMDtR1KY38UwVwW6LCt8AcY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP663039.RALCTmfLwE1rGl2-pj8r-lEMDtR1KY38UwVwW6LCt8AcY130_provenance.