Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP174178.RAUVqHfba1T-Nu20zUjQBps8MhwH5NmDW64m1S5fH5FTM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP174178.RAUVqHfba1T-Nu20zUjQBps8MhwH5NmDW64m1S5fH5FTM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP174178.RAUVqHfba1T-Nu20zUjQBps8MhwH5NmDW64m1S5fH5FTM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP174178.RAUVqHfba1T-Nu20zUjQBps8MhwH5NmDW64m1S5fH5FTM130_provenance.
- NP174178.RAUVqHfba1T-Nu20zUjQBps8MhwH5NmDW64m1S5fH5FTM130_assertion description "[Mutations in the Notch pathway ligand Jagged1 (JAG1) cause Alagille syndrome (AGS), as well as cardiac defects in seemingly nonsyndromic individuals.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP174178.RAUVqHfba1T-Nu20zUjQBps8MhwH5NmDW64m1S5fH5FTM130_provenance.
- NP174178.RAUVqHfba1T-Nu20zUjQBps8MhwH5NmDW64m1S5fH5FTM130_assertion evidence source_evidence_literature NP174178.RAUVqHfba1T-Nu20zUjQBps8MhwH5NmDW64m1S5fH5FTM130_provenance.
- NP174178.RAUVqHfba1T-Nu20zUjQBps8MhwH5NmDW64m1S5fH5FTM130_assertion SIO_000772 20437614 NP174178.RAUVqHfba1T-Nu20zUjQBps8MhwH5NmDW64m1S5fH5FTM130_provenance.
- NP174178.RAUVqHfba1T-Nu20zUjQBps8MhwH5NmDW64m1S5fH5FTM130_assertion wasDerivedFrom gad-20150221 NP174178.RAUVqHfba1T-Nu20zUjQBps8MhwH5NmDW64m1S5fH5FTM130_provenance.
- NP174178.RAUVqHfba1T-Nu20zUjQBps8MhwH5NmDW64m1S5fH5FTM130_assertion wasGeneratedBy ECO_0000203 NP174178.RAUVqHfba1T-Nu20zUjQBps8MhwH5NmDW64m1S5fH5FTM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP174178.RAUVqHfba1T-Nu20zUjQBps8MhwH5NmDW64m1S5fH5FTM130_provenance.