Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP394727.RABHH-mu7efrmDC516c-AqtN5ZWtJ9CkJnsLjtYdCA4Eg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP394727.RABHH-mu7efrmDC516c-AqtN5ZWtJ9CkJnsLjtYdCA4Eg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP394727.RABHH-mu7efrmDC516c-AqtN5ZWtJ9CkJnsLjtYdCA4Eg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP394727.RABHH-mu7efrmDC516c-AqtN5ZWtJ9CkJnsLjtYdCA4Eg130_provenance.
- NP394727.RABHH-mu7efrmDC516c-AqtN5ZWtJ9CkJnsLjtYdCA4Eg130_assertion description "[As a first step in understanding the pathophysiology of AVMs, the authors investigated the hypothesis that endothelial dysfunction-specifically, deregulation of endothelin-1 (ET-1) secretion-contributes to the abnormal vascular phenotype and the lack of hemodynamic autoregulation elaborated by these lesions.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP394727.RABHH-mu7efrmDC516c-AqtN5ZWtJ9CkJnsLjtYdCA4Eg130_provenance.
- NP394727.RABHH-mu7efrmDC516c-AqtN5ZWtJ9CkJnsLjtYdCA4Eg130_assertion evidence source_evidence_literature NP394727.RABHH-mu7efrmDC516c-AqtN5ZWtJ9CkJnsLjtYdCA4Eg130_provenance.
- NP394727.RABHH-mu7efrmDC516c-AqtN5ZWtJ9CkJnsLjtYdCA4Eg130_assertion SIO_000772 8988087 NP394727.RABHH-mu7efrmDC516c-AqtN5ZWtJ9CkJnsLjtYdCA4Eg130_provenance.
- NP394727.RABHH-mu7efrmDC516c-AqtN5ZWtJ9CkJnsLjtYdCA4Eg130_assertion wasDerivedFrom befree-20140225 NP394727.RABHH-mu7efrmDC516c-AqtN5ZWtJ9CkJnsLjtYdCA4Eg130_provenance.
- NP394727.RABHH-mu7efrmDC516c-AqtN5ZWtJ9CkJnsLjtYdCA4Eg130_assertion wasGeneratedBy ECO_0000203 NP394727.RABHH-mu7efrmDC516c-AqtN5ZWtJ9CkJnsLjtYdCA4Eg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP394727.RABHH-mu7efrmDC516c-AqtN5ZWtJ9CkJnsLjtYdCA4Eg130_provenance.