Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_provenance.
- NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_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." NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_provenance.
- NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_assertion evidence source_evidence_literature NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_provenance.
- NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_assertion SIO_000772 16429404 NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_provenance.
- NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_assertion wasDerivedFrom befree-20150227 NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_provenance.
- NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_assertion wasGeneratedBy ECO_0000203 NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_provenance.
- befree-20150227 importedOn "2015-02-27" NP374779.RAFvXlNgI-_1HYh0y0VwPfsNb1h6jEiVzsbh_ElssB1XU130_provenance.