Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP523692.RA6WAODFspeDFJHDHuCREBovZmpp39x0AY_QB36H5W_7Q130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP523692.RA6WAODFspeDFJHDHuCREBovZmpp39x0AY_QB36H5W_7Q130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP523692.RA6WAODFspeDFJHDHuCREBovZmpp39x0AY_QB36H5W_7Q130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP523692.RA6WAODFspeDFJHDHuCREBovZmpp39x0AY_QB36H5W_7Q130_provenance.
- NP523692.RA6WAODFspeDFJHDHuCREBovZmpp39x0AY_QB36H5W_7Q130_assertion description "[We report about the partial de novo loss of GLRB and GRIA2 in an individual with intellectual disability (ID).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP523692.RA6WAODFspeDFJHDHuCREBovZmpp39x0AY_QB36H5W_7Q130_provenance.
- NP523692.RA6WAODFspeDFJHDHuCREBovZmpp39x0AY_QB36H5W_7Q130_assertion evidence source_evidence_literature NP523692.RA6WAODFspeDFJHDHuCREBovZmpp39x0AY_QB36H5W_7Q130_provenance.
- NP523692.RA6WAODFspeDFJHDHuCREBovZmpp39x0AY_QB36H5W_7Q130_assertion SIO_000772 22669415 NP523692.RA6WAODFspeDFJHDHuCREBovZmpp39x0AY_QB36H5W_7Q130_provenance.
- NP523692.RA6WAODFspeDFJHDHuCREBovZmpp39x0AY_QB36H5W_7Q130_assertion wasDerivedFrom befree-20140225 NP523692.RA6WAODFspeDFJHDHuCREBovZmpp39x0AY_QB36H5W_7Q130_provenance.
- NP523692.RA6WAODFspeDFJHDHuCREBovZmpp39x0AY_QB36H5W_7Q130_assertion wasGeneratedBy ECO_0000203 NP523692.RA6WAODFspeDFJHDHuCREBovZmpp39x0AY_QB36H5W_7Q130_provenance.
- befree-20140225 importedOn "2014-02-25" NP523692.RA6WAODFspeDFJHDHuCREBovZmpp39x0AY_QB36H5W_7Q130_provenance.