Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP807020.RA4gPcBzW4UrtmTphzuzcuKREZryTFfoYIuObBrXEgRr0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP807020.RA4gPcBzW4UrtmTphzuzcuKREZryTFfoYIuObBrXEgRr0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP807020.RA4gPcBzW4UrtmTphzuzcuKREZryTFfoYIuObBrXEgRr0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP807020.RA4gPcBzW4UrtmTphzuzcuKREZryTFfoYIuObBrXEgRr0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP807020.RA4gPcBzW4UrtmTphzuzcuKREZryTFfoYIuObBrXEgRr0130_provenance.
- NP807020.RA4gPcBzW4UrtmTphzuzcuKREZryTFfoYIuObBrXEgRr0130_assertion wasGeneratedBy ECO_0000203 NP807020.RA4gPcBzW4UrtmTphzuzcuKREZryTFfoYIuObBrXEgRr0130_provenance.
- NP807020.RA4gPcBzW4UrtmTphzuzcuKREZryTFfoYIuObBrXEgRr0130_assertion wasDerivedFrom befree-20150227 NP807020.RA4gPcBzW4UrtmTphzuzcuKREZryTFfoYIuObBrXEgRr0130_provenance.
- NP807020.RA4gPcBzW4UrtmTphzuzcuKREZryTFfoYIuObBrXEgRr0130_assertion SIO_000772 18363760 NP807020.RA4gPcBzW4UrtmTphzuzcuKREZryTFfoYIuObBrXEgRr0130_provenance.
- NP807020.RA4gPcBzW4UrtmTphzuzcuKREZryTFfoYIuObBrXEgRr0130_assertion evidence source_evidence_literature NP807020.RA4gPcBzW4UrtmTphzuzcuKREZryTFfoYIuObBrXEgRr0130_provenance.
- NP807020.RA4gPcBzW4UrtmTphzuzcuKREZryTFfoYIuObBrXEgRr0130_assertion description "[We have demonstrated that the spectrum of clinical manifestations due to mutations in RASA1 is wider than previously thought and also includes typical CMs not associated with AVM/AVF.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP807020.RA4gPcBzW4UrtmTphzuzcuKREZryTFfoYIuObBrXEgRr0130_provenance.