Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_provenance.
- NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_assertion description "[The CC2D1A, a member of a new gene family with C2 domains, is involved in autosomal recessive non-syndromic mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_provenance.
- NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_assertion evidence source_evidence_literature NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_provenance.
- NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_assertion SIO_000772 16033914 NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_provenance.
- NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_assertion wasDerivedFrom befree-20150227 NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_provenance.
- NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_assertion wasGeneratedBy ECO_0000203 NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_provenance.
- befree-20150227 importedOn "2015-02-27" NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_provenance.