Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP717074.RADHhdXOQzSV4cGIpBt9OcOaNH_bg8QHQwGxEVH1MSTdQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP717074.RADHhdXOQzSV4cGIpBt9OcOaNH_bg8QHQwGxEVH1MSTdQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP717074.RADHhdXOQzSV4cGIpBt9OcOaNH_bg8QHQwGxEVH1MSTdQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP717074.RADHhdXOQzSV4cGIpBt9OcOaNH_bg8QHQwGxEVH1MSTdQ130_provenance.
- NP717074.RADHhdXOQzSV4cGIpBt9OcOaNH_bg8QHQwGxEVH1MSTdQ130_assertion description "[Mutations of human jagged 1 (JAG1) gene are responsible for Alagille Syndrome (AGS), whose 2 main symptoms are intrahepatic bile duct hypoplasia and pulmonary stenosis.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP717074.RADHhdXOQzSV4cGIpBt9OcOaNH_bg8QHQwGxEVH1MSTdQ130_provenance.
- NP717074.RADHhdXOQzSV4cGIpBt9OcOaNH_bg8QHQwGxEVH1MSTdQ130_assertion evidence source_evidence_literature NP717074.RADHhdXOQzSV4cGIpBt9OcOaNH_bg8QHQwGxEVH1MSTdQ130_provenance.
- NP717074.RADHhdXOQzSV4cGIpBt9OcOaNH_bg8QHQwGxEVH1MSTdQ130_assertion SIO_000772 12297837 NP717074.RADHhdXOQzSV4cGIpBt9OcOaNH_bg8QHQwGxEVH1MSTdQ130_provenance.
- NP717074.RADHhdXOQzSV4cGIpBt9OcOaNH_bg8QHQwGxEVH1MSTdQ130_assertion wasDerivedFrom befree-20140225 NP717074.RADHhdXOQzSV4cGIpBt9OcOaNH_bg8QHQwGxEVH1MSTdQ130_provenance.
- NP717074.RADHhdXOQzSV4cGIpBt9OcOaNH_bg8QHQwGxEVH1MSTdQ130_assertion wasGeneratedBy ECO_0000203 NP717074.RADHhdXOQzSV4cGIpBt9OcOaNH_bg8QHQwGxEVH1MSTdQ130_provenance.
- befree-20140225 importedOn "2014-02-25" NP717074.RADHhdXOQzSV4cGIpBt9OcOaNH_bg8QHQwGxEVH1MSTdQ130_provenance.