Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP490240.RAcwVwBzlz-k6k4pkNC5qOjXDXodbLJriQ_TdS2npfi5w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP490240.RAcwVwBzlz-k6k4pkNC5qOjXDXodbLJriQ_TdS2npfi5w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP490240.RAcwVwBzlz-k6k4pkNC5qOjXDXodbLJriQ_TdS2npfi5w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP490240.RAcwVwBzlz-k6k4pkNC5qOjXDXodbLJriQ_TdS2npfi5w130_provenance.
- NP490240.RAcwVwBzlz-k6k4pkNC5qOjXDXodbLJriQ_TdS2npfi5w130_assertion wasGeneratedBy ECO_0000203 NP490240.RAcwVwBzlz-k6k4pkNC5qOjXDXodbLJriQ_TdS2npfi5w130_provenance.
- NP490240.RAcwVwBzlz-k6k4pkNC5qOjXDXodbLJriQ_TdS2npfi5w130_assertion wasDerivedFrom befree-20140225 NP490240.RAcwVwBzlz-k6k4pkNC5qOjXDXodbLJriQ_TdS2npfi5w130_provenance.
- NP490240.RAcwVwBzlz-k6k4pkNC5qOjXDXodbLJriQ_TdS2npfi5w130_assertion SIO_000772 11181572 NP490240.RAcwVwBzlz-k6k4pkNC5qOjXDXodbLJriQ_TdS2npfi5w130_provenance.
- NP490240.RAcwVwBzlz-k6k4pkNC5qOjXDXodbLJriQ_TdS2npfi5w130_assertion evidence source_evidence_literature NP490240.RAcwVwBzlz-k6k4pkNC5qOjXDXodbLJriQ_TdS2npfi5w130_provenance.
- NP490240.RAcwVwBzlz-k6k4pkNC5qOjXDXodbLJriQ_TdS2npfi5w130_assertion description "[FGD1, the gene responsible for the inherited disease faciogenital dysplasia, encodes a guanine nucleotide exchange factor (GEF) that specifically activates the p21 GTPase Cdc42.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP490240.RAcwVwBzlz-k6k4pkNC5qOjXDXodbLJriQ_TdS2npfi5w130_provenance.
- befree-20140225 importedOn "2014-02-25" NP490240.RAcwVwBzlz-k6k4pkNC5qOjXDXodbLJriQ_TdS2npfi5w130_provenance.