Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_provenance.
- NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_assertion description "[Mutations in vascular endothelial growth factor (VEGF) receptor-3 (VEGFR3 or FLT4) cause Milroy disease, an autosomal dominant condition that presents with congenital lymphedema.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_provenance.
- NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_assertion evidence source_evidence_literature NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_provenance.
- NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_assertion SIO_000772 23410910 NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_provenance.
- NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_assertion wasDerivedFrom befree-20150227 NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_provenance.
- NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_assertion wasGeneratedBy ECO_0000203 NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_provenance.
- befree-20150227 importedOn "2015-02-27" NP772732.RA3jG6_S6uu8dDgvuW7wVJ3Xntbia8lppp4gyb0HQrA9E130_provenance.