Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP623987.RAqllH_A5GNXaVgWdqbGnKqLzV-CioE5Xpv2E4o3K9gCs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP623987.RAqllH_A5GNXaVgWdqbGnKqLzV-CioE5Xpv2E4o3K9gCs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP623987.RAqllH_A5GNXaVgWdqbGnKqLzV-CioE5Xpv2E4o3K9gCs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP623987.RAqllH_A5GNXaVgWdqbGnKqLzV-CioE5Xpv2E4o3K9gCs130_provenance.
- NP623987.RAqllH_A5GNXaVgWdqbGnKqLzV-CioE5Xpv2E4o3K9gCs130_assertion description "[Germline NF1, c-RET, SDH, and VHL mutations cause familial pheochromocytoma.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP623987.RAqllH_A5GNXaVgWdqbGnKqLzV-CioE5Xpv2E4o3K9gCs130_provenance.
- NP623987.RAqllH_A5GNXaVgWdqbGnKqLzV-CioE5Xpv2E4o3K9gCs130_assertion evidence source_evidence_literature NP623987.RAqllH_A5GNXaVgWdqbGnKqLzV-CioE5Xpv2E4o3K9gCs130_provenance.
- NP623987.RAqllH_A5GNXaVgWdqbGnKqLzV-CioE5Xpv2E4o3K9gCs130_assertion SIO_000772 16098468 NP623987.RAqllH_A5GNXaVgWdqbGnKqLzV-CioE5Xpv2E4o3K9gCs130_provenance.
- NP623987.RAqllH_A5GNXaVgWdqbGnKqLzV-CioE5Xpv2E4o3K9gCs130_assertion wasDerivedFrom befree-20140225 NP623987.RAqllH_A5GNXaVgWdqbGnKqLzV-CioE5Xpv2E4o3K9gCs130_provenance.
- NP623987.RAqllH_A5GNXaVgWdqbGnKqLzV-CioE5Xpv2E4o3K9gCs130_assertion wasGeneratedBy ECO_0000203 NP623987.RAqllH_A5GNXaVgWdqbGnKqLzV-CioE5Xpv2E4o3K9gCs130_provenance.
- befree-20140225 importedOn "2014-02-25" NP623987.RAqllH_A5GNXaVgWdqbGnKqLzV-CioE5Xpv2E4o3K9gCs130_provenance.