Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP387957.RAwRBu33C1l_Y43k-Lj6fdCdsIyhgSUPQy_ZF3iQEcxFA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP387957.RAwRBu33C1l_Y43k-Lj6fdCdsIyhgSUPQy_ZF3iQEcxFA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP387957.RAwRBu33C1l_Y43k-Lj6fdCdsIyhgSUPQy_ZF3iQEcxFA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP387957.RAwRBu33C1l_Y43k-Lj6fdCdsIyhgSUPQy_ZF3iQEcxFA130_provenance.
- befree-2016 importedOn "2016-02-19" NP387957.RAwRBu33C1l_Y43k-Lj6fdCdsIyhgSUPQy_ZF3iQEcxFA130_provenance.
- NP387957.RAwRBu33C1l_Y43k-Lj6fdCdsIyhgSUPQy_ZF3iQEcxFA130_assertion wasGeneratedBy ECO_0000203 NP387957.RAwRBu33C1l_Y43k-Lj6fdCdsIyhgSUPQy_ZF3iQEcxFA130_provenance.
- NP387957.RAwRBu33C1l_Y43k-Lj6fdCdsIyhgSUPQy_ZF3iQEcxFA130_assertion wasDerivedFrom befree-2016 NP387957.RAwRBu33C1l_Y43k-Lj6fdCdsIyhgSUPQy_ZF3iQEcxFA130_provenance.
- NP387957.RAwRBu33C1l_Y43k-Lj6fdCdsIyhgSUPQy_ZF3iQEcxFA130_assertion SIO_000772 12649809 NP387957.RAwRBu33C1l_Y43k-Lj6fdCdsIyhgSUPQy_ZF3iQEcxFA130_provenance.
- NP387957.RAwRBu33C1l_Y43k-Lj6fdCdsIyhgSUPQy_ZF3iQEcxFA130_assertion evidence source_evidence_literature NP387957.RAwRBu33C1l_Y43k-Lj6fdCdsIyhgSUPQy_ZF3iQEcxFA130_provenance.
- NP387957.RAwRBu33C1l_Y43k-Lj6fdCdsIyhgSUPQy_ZF3iQEcxFA130_assertion description "[We have studied a JAG1 missense mutation (JAG1-G274D) that was previously identified in 13 individuals from an extended family with cardiac defects of the type seen in patients with AGS (e.g., peripheral pulmonic stenosis and tetralogy of Fallot) in the absence of liver dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP387957.RAwRBu33C1l_Y43k-Lj6fdCdsIyhgSUPQy_ZF3iQEcxFA130_provenance.