Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP790244.RAdFXNiha1Rb-1iQMJWdUJDfnUFskQ26ZzYstpr960U2M130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP790244.RAdFXNiha1Rb-1iQMJWdUJDfnUFskQ26ZzYstpr960U2M130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP790244.RAdFXNiha1Rb-1iQMJWdUJDfnUFskQ26ZzYstpr960U2M130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP790244.RAdFXNiha1Rb-1iQMJWdUJDfnUFskQ26ZzYstpr960U2M130_provenance.
- NP790244.RAdFXNiha1Rb-1iQMJWdUJDfnUFskQ26ZzYstpr960U2M130_assertion wasGeneratedBy ECO_0000203 NP790244.RAdFXNiha1Rb-1iQMJWdUJDfnUFskQ26ZzYstpr960U2M130_provenance.
- NP790244.RAdFXNiha1Rb-1iQMJWdUJDfnUFskQ26ZzYstpr960U2M130_assertion wasDerivedFrom befree-20140225 NP790244.RAdFXNiha1Rb-1iQMJWdUJDfnUFskQ26ZzYstpr960U2M130_provenance.
- NP790244.RAdFXNiha1Rb-1iQMJWdUJDfnUFskQ26ZzYstpr960U2M130_assertion SIO_000772 17575113 NP790244.RAdFXNiha1Rb-1iQMJWdUJDfnUFskQ26ZzYstpr960U2M130_provenance.
- NP790244.RAdFXNiha1Rb-1iQMJWdUJDfnUFskQ26ZzYstpr960U2M130_assertion evidence source_evidence_literature NP790244.RAdFXNiha1Rb-1iQMJWdUJDfnUFskQ26ZzYstpr960U2M130_provenance.
- NP790244.RAdFXNiha1Rb-1iQMJWdUJDfnUFskQ26ZzYstpr960U2M130_assertion description "[GPR56 is an orphan G protein - coupled receptor, mutations of which have recently been associated with bilateral frontoparietal polymicrogyria, a rare neurologic disease that has implications in brain development.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP790244.RAdFXNiha1Rb-1iQMJWdUJDfnUFskQ26ZzYstpr960U2M130_provenance.
- befree-20140225 importedOn "2014-02-25" NP790244.RAdFXNiha1Rb-1iQMJWdUJDfnUFskQ26ZzYstpr960U2M130_provenance.