Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_assertion> ?p ?o ?g. }
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- NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_assertion type Assertion NP914961.RAmo9NZT5p5ltRE5mT6ffcPZCDuUsRPQLonS72DcRq4f0130_head.
- 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.