Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_assertion> ?p ?o ?g. }
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- NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_assertion type Assertion NP597185.RAVo_HsNHU1SsNcPs7D8oslB7xQxRbHr-6GjRtX38wemk130_head.
- 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.