Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP368792.RAP24x73cuw9g-iSgPyUHbPj-bPgXMiYv2yPxYrqxP3Dw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP368792.RAP24x73cuw9g-iSgPyUHbPj-bPgXMiYv2yPxYrqxP3Dw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP368792.RAP24x73cuw9g-iSgPyUHbPj-bPgXMiYv2yPxYrqxP3Dw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP368792.RAP24x73cuw9g-iSgPyUHbPj-bPgXMiYv2yPxYrqxP3Dw130_provenance.
- befree-2016 importedOn "2016-02-19" NP368792.RAP24x73cuw9g-iSgPyUHbPj-bPgXMiYv2yPxYrqxP3Dw130_provenance.
- NP368792.RAP24x73cuw9g-iSgPyUHbPj-bPgXMiYv2yPxYrqxP3Dw130_assertion wasGeneratedBy ECO_0000203 NP368792.RAP24x73cuw9g-iSgPyUHbPj-bPgXMiYv2yPxYrqxP3Dw130_provenance.
- NP368792.RAP24x73cuw9g-iSgPyUHbPj-bPgXMiYv2yPxYrqxP3Dw130_assertion wasDerivedFrom befree-2016 NP368792.RAP24x73cuw9g-iSgPyUHbPj-bPgXMiYv2yPxYrqxP3Dw130_provenance.
- NP368792.RAP24x73cuw9g-iSgPyUHbPj-bPgXMiYv2yPxYrqxP3Dw130_assertion SIO_000772 12297837 NP368792.RAP24x73cuw9g-iSgPyUHbPj-bPgXMiYv2yPxYrqxP3Dw130_provenance.
- NP368792.RAP24x73cuw9g-iSgPyUHbPj-bPgXMiYv2yPxYrqxP3Dw130_assertion evidence source_evidence_literature NP368792.RAP24x73cuw9g-iSgPyUHbPj-bPgXMiYv2yPxYrqxP3Dw130_provenance.
- NP368792.RAP24x73cuw9g-iSgPyUHbPj-bPgXMiYv2yPxYrqxP3Dw130_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." NP368792.RAP24x73cuw9g-iSgPyUHbPj-bPgXMiYv2yPxYrqxP3Dw130_provenance.