Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1207962.RAIl3P_NSxnF-BZYR5_U2_B1eh2Mr57dIX0rSgXXN29hE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1207962.RAIl3P_NSxnF-BZYR5_U2_B1eh2Mr57dIX0rSgXXN29hE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1207962.RAIl3P_NSxnF-BZYR5_U2_B1eh2Mr57dIX0rSgXXN29hE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1207962.RAIl3P_NSxnF-BZYR5_U2_B1eh2Mr57dIX0rSgXXN29hE130_provenance.
- NP1207962.RAIl3P_NSxnF-BZYR5_U2_B1eh2Mr57dIX0rSgXXN29hE130_assertion description "[This is the first report of a functionally significant HAND2 mutation in a patient with congenital heart disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1207962.RAIl3P_NSxnF-BZYR5_U2_B1eh2Mr57dIX0rSgXXN29hE130_provenance.
- NP1207962.RAIl3P_NSxnF-BZYR5_U2_B1eh2Mr57dIX0rSgXXN29hE130_assertion evidence source_evidence_literature NP1207962.RAIl3P_NSxnF-BZYR5_U2_B1eh2Mr57dIX0rSgXXN29hE130_provenance.
- NP1207962.RAIl3P_NSxnF-BZYR5_U2_B1eh2Mr57dIX0rSgXXN29hE130_assertion SIO_000772 25093829 NP1207962.RAIl3P_NSxnF-BZYR5_U2_B1eh2Mr57dIX0rSgXXN29hE130_provenance.
- NP1207962.RAIl3P_NSxnF-BZYR5_U2_B1eh2Mr57dIX0rSgXXN29hE130_assertion wasDerivedFrom befree-2016 NP1207962.RAIl3P_NSxnF-BZYR5_U2_B1eh2Mr57dIX0rSgXXN29hE130_provenance.
- NP1207962.RAIl3P_NSxnF-BZYR5_U2_B1eh2Mr57dIX0rSgXXN29hE130_assertion wasGeneratedBy ECO_0000203 NP1207962.RAIl3P_NSxnF-BZYR5_U2_B1eh2Mr57dIX0rSgXXN29hE130_provenance.
- befree-2016 importedOn "2016-02-19" NP1207962.RAIl3P_NSxnF-BZYR5_U2_B1eh2Mr57dIX0rSgXXN29hE130_provenance.