Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_provenance.
- befree-2016 importedOn "2016-02-19" NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_provenance.
- NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_assertion wasGeneratedBy ECO_0000203 NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_provenance.
- NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_assertion wasDerivedFrom befree-2016 NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_provenance.
- NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_assertion SIO_000772 16470787 NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_provenance.
- NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_assertion evidence source_evidence_literature NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_provenance.
- NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_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." NP535450.RA_4M7Tsw07wHE8TM_Iv0-By9VwVCYVCn9XQ5PkKBV9lE130_provenance.