Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP799143.RASlgGtliMZ41jPnkGA2Sp5_oLvnw1FGza7UFK-MXyENg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP799143.RASlgGtliMZ41jPnkGA2Sp5_oLvnw1FGza7UFK-MXyENg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP799143.RASlgGtliMZ41jPnkGA2Sp5_oLvnw1FGza7UFK-MXyENg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP799143.RASlgGtliMZ41jPnkGA2Sp5_oLvnw1FGza7UFK-MXyENg130_provenance.
- NP799143.RASlgGtliMZ41jPnkGA2Sp5_oLvnw1FGza7UFK-MXyENg130_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." NP799143.RASlgGtliMZ41jPnkGA2Sp5_oLvnw1FGza7UFK-MXyENg130_provenance.
- NP799143.RASlgGtliMZ41jPnkGA2Sp5_oLvnw1FGza7UFK-MXyENg130_assertion evidence source_evidence_literature NP799143.RASlgGtliMZ41jPnkGA2Sp5_oLvnw1FGza7UFK-MXyENg130_provenance.
- NP799143.RASlgGtliMZ41jPnkGA2Sp5_oLvnw1FGza7UFK-MXyENg130_assertion SIO_000772 16098468 NP799143.RASlgGtliMZ41jPnkGA2Sp5_oLvnw1FGza7UFK-MXyENg130_provenance.
- NP799143.RASlgGtliMZ41jPnkGA2Sp5_oLvnw1FGza7UFK-MXyENg130_assertion wasDerivedFrom befree-20140225 NP799143.RASlgGtliMZ41jPnkGA2Sp5_oLvnw1FGza7UFK-MXyENg130_provenance.
- NP799143.RASlgGtliMZ41jPnkGA2Sp5_oLvnw1FGza7UFK-MXyENg130_assertion wasGeneratedBy ECO_0000203 NP799143.RASlgGtliMZ41jPnkGA2Sp5_oLvnw1FGza7UFK-MXyENg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP799143.RASlgGtliMZ41jPnkGA2Sp5_oLvnw1FGza7UFK-MXyENg130_provenance.