Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_provenance.
- NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_assertion description "[Hereditary haemorrhagic telangiectasia (HHT or Rendu-Osler-Weber syndrome) is an autosomal dominant disorder characterized by localized angiodysplasia due to mutations in endoglin, ALK-1 gene, and a still unidentified locus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_provenance.
- NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_assertion evidence source_evidence_literature NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_provenance.
- NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_assertion SIO_000772 16429404 NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_provenance.
- NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_assertion wasDerivedFrom befree-20140225 NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_provenance.
- NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_assertion wasGeneratedBy ECO_0000203 NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP704391.RA_G2pAVAd4QQUhXDkuf02TH5z0C53BnVMtJMzWuEmkYA130_provenance.