Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_provenance.
- NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_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." NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_provenance.
- NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_assertion evidence source_evidence_literature NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_provenance.
- NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_assertion SIO_000772 16429404 NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_provenance.
- NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_assertion wasDerivedFrom befree-20140225 NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_provenance.
- NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_assertion wasGeneratedBy ECO_0000203 NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_provenance.