Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_provenance.
- befree-20150227 importedOn "2015-02-27" NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_provenance.
- NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_assertion wasGeneratedBy ECO_0000203 NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_provenance.
- NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_assertion wasDerivedFrom befree-20150227 NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_provenance.
- NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_assertion SIO_000772 16470787 NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_provenance.
- NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_assertion evidence source_evidence_literature NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_provenance.
- NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is a genetically heterogeneous vascular dysplasia with multiple telangiectases and arteriovenous malformations and it is caused by mutations in endoglin gene (ENG) (HHT1) and activin A receptor type II-like 1 gene (ACVRL1) (HHT2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP374626.RAl8Ay5YK3wNZ9t0oljDOWECEt3tmfu9lOU1MVUVV245c130_provenance.