Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP642190.RAKeelbmm0Ud135IrGVbo2XzJWUCtK9dDl4TJUb3Es2IQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP642190.RAKeelbmm0Ud135IrGVbo2XzJWUCtK9dDl4TJUb3Es2IQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP642190.RAKeelbmm0Ud135IrGVbo2XzJWUCtK9dDl4TJUb3Es2IQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP642190.RAKeelbmm0Ud135IrGVbo2XzJWUCtK9dDl4TJUb3Es2IQ130_provenance.
- NP642190.RAKeelbmm0Ud135IrGVbo2XzJWUCtK9dDl4TJUb3Es2IQ130_assertion description "[Genetic testing of the 2 sisters and their mother (who also had multiple facial lentigines but did not have Cushing syndrome) revealed a novel mutation in the PRKAR1A gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP642190.RAKeelbmm0Ud135IrGVbo2XzJWUCtK9dDl4TJUb3Es2IQ130_provenance.
- NP642190.RAKeelbmm0Ud135IrGVbo2XzJWUCtK9dDl4TJUb3Es2IQ130_assertion evidence source_evidence_literature NP642190.RAKeelbmm0Ud135IrGVbo2XzJWUCtK9dDl4TJUb3Es2IQ130_provenance.
- NP642190.RAKeelbmm0Ud135IrGVbo2XzJWUCtK9dDl4TJUb3Es2IQ130_assertion SIO_000772 19833579 NP642190.RAKeelbmm0Ud135IrGVbo2XzJWUCtK9dDl4TJUb3Es2IQ130_provenance.
- NP642190.RAKeelbmm0Ud135IrGVbo2XzJWUCtK9dDl4TJUb3Es2IQ130_assertion wasDerivedFrom befree-20150227 NP642190.RAKeelbmm0Ud135IrGVbo2XzJWUCtK9dDl4TJUb3Es2IQ130_provenance.
- NP642190.RAKeelbmm0Ud135IrGVbo2XzJWUCtK9dDl4TJUb3Es2IQ130_assertion wasGeneratedBy ECO_0000203 NP642190.RAKeelbmm0Ud135IrGVbo2XzJWUCtK9dDl4TJUb3Es2IQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP642190.RAKeelbmm0Ud135IrGVbo2XzJWUCtK9dDl4TJUb3Es2IQ130_provenance.