Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_provenance.
- NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_assertion description "[Hereditary hemorrhagic telangiectasia (HHT) is an autosomal dominant and age-dependent vascular disorder originated by mutations in Endoglin (ENG) or activin receptor-like kinase-1 (ALK1, ACVRL1) genes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_provenance.
- NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_assertion evidence source_evidence_literature NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_provenance.
- NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_assertion SIO_000772 16470589 NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_provenance.
- NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_assertion wasDerivedFrom befree-20140225 NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_provenance.
- NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_assertion wasGeneratedBy ECO_0000203 NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP469104.RAdjY8n1jByABc8zwujS3mlIGKOx6_1Si5-nOmLyaVQjE130_provenance.