Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP140682.RAdXgTe0E7hydoDIG1-NIlx1Ep1gfWGVMY4bupxgOxpUE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP140682.RAdXgTe0E7hydoDIG1-NIlx1Ep1gfWGVMY4bupxgOxpUE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP140682.RAdXgTe0E7hydoDIG1-NIlx1Ep1gfWGVMY4bupxgOxpUE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP140682.RAdXgTe0E7hydoDIG1-NIlx1Ep1gfWGVMY4bupxgOxpUE130_provenance.
- NP140682.RAdXgTe0E7hydoDIG1-NIlx1Ep1gfWGVMY4bupxgOxpUE130_assertion description "[Germline BRAF mutations in Noonan, LEOPARD, and cardiofaciocutaneous syndromes: molecular diversity and associated phenotypic spectrum.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP140682.RAdXgTe0E7hydoDIG1-NIlx1Ep1gfWGVMY4bupxgOxpUE130_provenance.
- NP140682.RAdXgTe0E7hydoDIG1-NIlx1Ep1gfWGVMY4bupxgOxpUE130_assertion evidence source_evidence_literature NP140682.RAdXgTe0E7hydoDIG1-NIlx1Ep1gfWGVMY4bupxgOxpUE130_provenance.
- NP140682.RAdXgTe0E7hydoDIG1-NIlx1Ep1gfWGVMY4bupxgOxpUE130_assertion SIO_000772 19206169 NP140682.RAdXgTe0E7hydoDIG1-NIlx1Ep1gfWGVMY4bupxgOxpUE130_provenance.
- NP140682.RAdXgTe0E7hydoDIG1-NIlx1Ep1gfWGVMY4bupxgOxpUE130_assertion wasDerivedFrom gad-20150221 NP140682.RAdXgTe0E7hydoDIG1-NIlx1Ep1gfWGVMY4bupxgOxpUE130_provenance.
- NP140682.RAdXgTe0E7hydoDIG1-NIlx1Ep1gfWGVMY4bupxgOxpUE130_assertion wasGeneratedBy ECO_0000203 NP140682.RAdXgTe0E7hydoDIG1-NIlx1Ep1gfWGVMY4bupxgOxpUE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP140682.RAdXgTe0E7hydoDIG1-NIlx1Ep1gfWGVMY4bupxgOxpUE130_provenance.