Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP682579.RAmb5Q5-pjRBk2tMtVxtHjvVkuRA8TmplUs06oELdy5Os130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682579.RAmb5Q5-pjRBk2tMtVxtHjvVkuRA8TmplUs06oELdy5Os130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682579.RAmb5Q5-pjRBk2tMtVxtHjvVkuRA8TmplUs06oELdy5Os130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682579.RAmb5Q5-pjRBk2tMtVxtHjvVkuRA8TmplUs06oELdy5Os130_provenance.
- NP682579.RAmb5Q5-pjRBk2tMtVxtHjvVkuRA8TmplUs06oELdy5Os130_assertion description "[In one of the patients, the PRKAR1A gene responsible for Carney Complex and the KCNJ2 gene causal for Andersen syndrome are deleted.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682579.RAmb5Q5-pjRBk2tMtVxtHjvVkuRA8TmplUs06oELdy5Os130_provenance.
- NP682579.RAmb5Q5-pjRBk2tMtVxtHjvVkuRA8TmplUs06oELdy5Os130_assertion evidence source_evidence_literature NP682579.RAmb5Q5-pjRBk2tMtVxtHjvVkuRA8TmplUs06oELdy5Os130_provenance.
- NP682579.RAmb5Q5-pjRBk2tMtVxtHjvVkuRA8TmplUs06oELdy5Os130_assertion SIO_000772 22166941 NP682579.RAmb5Q5-pjRBk2tMtVxtHjvVkuRA8TmplUs06oELdy5Os130_provenance.
- NP682579.RAmb5Q5-pjRBk2tMtVxtHjvVkuRA8TmplUs06oELdy5Os130_assertion wasDerivedFrom befree-20140225 NP682579.RAmb5Q5-pjRBk2tMtVxtHjvVkuRA8TmplUs06oELdy5Os130_provenance.
- NP682579.RAmb5Q5-pjRBk2tMtVxtHjvVkuRA8TmplUs06oELdy5Os130_assertion wasGeneratedBy ECO_0000203 NP682579.RAmb5Q5-pjRBk2tMtVxtHjvVkuRA8TmplUs06oELdy5Os130_provenance.
- befree-20140225 importedOn "2014-02-25" NP682579.RAmb5Q5-pjRBk2tMtVxtHjvVkuRA8TmplUs06oELdy5Os130_provenance.