Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP773896.RAiKdz5h1nWXESwOf-PVvPojXW-94XBXVqYThRBRJUsxg130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP773896.RAiKdz5h1nWXESwOf-PVvPojXW-94XBXVqYThRBRJUsxg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP773896.RAiKdz5h1nWXESwOf-PVvPojXW-94XBXVqYThRBRJUsxg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP773896.RAiKdz5h1nWXESwOf-PVvPojXW-94XBXVqYThRBRJUsxg130_provenance.
- NP773896.RAiKdz5h1nWXESwOf-PVvPojXW-94XBXVqYThRBRJUsxg130_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." NP773896.RAiKdz5h1nWXESwOf-PVvPojXW-94XBXVqYThRBRJUsxg130_provenance.
- NP773896.RAiKdz5h1nWXESwOf-PVvPojXW-94XBXVqYThRBRJUsxg130_assertion evidence source_evidence_literature NP773896.RAiKdz5h1nWXESwOf-PVvPojXW-94XBXVqYThRBRJUsxg130_provenance.
- NP773896.RAiKdz5h1nWXESwOf-PVvPojXW-94XBXVqYThRBRJUsxg130_assertion SIO_000772 16098468 NP773896.RAiKdz5h1nWXESwOf-PVvPojXW-94XBXVqYThRBRJUsxg130_provenance.
- NP773896.RAiKdz5h1nWXESwOf-PVvPojXW-94XBXVqYThRBRJUsxg130_assertion wasDerivedFrom befree-20150227 NP773896.RAiKdz5h1nWXESwOf-PVvPojXW-94XBXVqYThRBRJUsxg130_provenance.
- NP773896.RAiKdz5h1nWXESwOf-PVvPojXW-94XBXVqYThRBRJUsxg130_assertion wasGeneratedBy ECO_0000203 NP773896.RAiKdz5h1nWXESwOf-PVvPojXW-94XBXVqYThRBRJUsxg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP773896.RAiKdz5h1nWXESwOf-PVvPojXW-94XBXVqYThRBRJUsxg130_provenance.