Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP373800.RA4sxDsPY_hpcJLRKVZJvoOGaIAPQ0SCqJK81gWtOMHFg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP373800.RA4sxDsPY_hpcJLRKVZJvoOGaIAPQ0SCqJK81gWtOMHFg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP373800.RA4sxDsPY_hpcJLRKVZJvoOGaIAPQ0SCqJK81gWtOMHFg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP373800.RA4sxDsPY_hpcJLRKVZJvoOGaIAPQ0SCqJK81gWtOMHFg130_provenance.
- NP373800.RA4sxDsPY_hpcJLRKVZJvoOGaIAPQ0SCqJK81gWtOMHFg130_assertion description "[Although the aetiology of Williams syndrome (WS) is related to elastin gene disruption, its pathogenesis remains unknown, particularly that of vascular lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP373800.RA4sxDsPY_hpcJLRKVZJvoOGaIAPQ0SCqJK81gWtOMHFg130_provenance.
- NP373800.RA4sxDsPY_hpcJLRKVZJvoOGaIAPQ0SCqJK81gWtOMHFg130_assertion evidence source_evidence_literature NP373800.RA4sxDsPY_hpcJLRKVZJvoOGaIAPQ0SCqJK81gWtOMHFg130_provenance.
- NP373800.RA4sxDsPY_hpcJLRKVZJvoOGaIAPQ0SCqJK81gWtOMHFg130_assertion SIO_000772 12095400 NP373800.RA4sxDsPY_hpcJLRKVZJvoOGaIAPQ0SCqJK81gWtOMHFg130_provenance.
- NP373800.RA4sxDsPY_hpcJLRKVZJvoOGaIAPQ0SCqJK81gWtOMHFg130_assertion wasDerivedFrom befree-20150227 NP373800.RA4sxDsPY_hpcJLRKVZJvoOGaIAPQ0SCqJK81gWtOMHFg130_provenance.
- NP373800.RA4sxDsPY_hpcJLRKVZJvoOGaIAPQ0SCqJK81gWtOMHFg130_assertion wasGeneratedBy ECO_0000203 NP373800.RA4sxDsPY_hpcJLRKVZJvoOGaIAPQ0SCqJK81gWtOMHFg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP373800.RA4sxDsPY_hpcJLRKVZJvoOGaIAPQ0SCqJK81gWtOMHFg130_provenance.