Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP952382.RAwVXwK84eQt-_LP_LCCnER5yS1cRdWuntSxp3VayAhjo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP952382.RAwVXwK84eQt-_LP_LCCnER5yS1cRdWuntSxp3VayAhjo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP952382.RAwVXwK84eQt-_LP_LCCnER5yS1cRdWuntSxp3VayAhjo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP952382.RAwVXwK84eQt-_LP_LCCnER5yS1cRdWuntSxp3VayAhjo130_provenance.
- NP952382.RAwVXwK84eQt-_LP_LCCnER5yS1cRdWuntSxp3VayAhjo130_assertion description "[Mutations in GPR56 cause a severe human brain malformation called bilateral frontoparietal polymicrogyria, in which neurons transmigrate through the BM causing severe mental retardation and frequent seizures.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP952382.RAwVXwK84eQt-_LP_LCCnER5yS1cRdWuntSxp3VayAhjo130_provenance.
- NP952382.RAwVXwK84eQt-_LP_LCCnER5yS1cRdWuntSxp3VayAhjo130_assertion evidence source_evidence_literature NP952382.RAwVXwK84eQt-_LP_LCCnER5yS1cRdWuntSxp3VayAhjo130_provenance.
- NP952382.RAwVXwK84eQt-_LP_LCCnER5yS1cRdWuntSxp3VayAhjo130_assertion SIO_000772 22235340 NP952382.RAwVXwK84eQt-_LP_LCCnER5yS1cRdWuntSxp3VayAhjo130_provenance.
- NP952382.RAwVXwK84eQt-_LP_LCCnER5yS1cRdWuntSxp3VayAhjo130_assertion wasDerivedFrom befree-2016 NP952382.RAwVXwK84eQt-_LP_LCCnER5yS1cRdWuntSxp3VayAhjo130_provenance.
- NP952382.RAwVXwK84eQt-_LP_LCCnER5yS1cRdWuntSxp3VayAhjo130_assertion wasGeneratedBy ECO_0000203 NP952382.RAwVXwK84eQt-_LP_LCCnER5yS1cRdWuntSxp3VayAhjo130_provenance.
- befree-2016 importedOn "2016-02-19" NP952382.RAwVXwK84eQt-_LP_LCCnER5yS1cRdWuntSxp3VayAhjo130_provenance.