Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP127006.RAVNRDxBq0Z-xwOUFoIcQLYcL3hrsmepIAyVdZI88Bnec130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP127006.RAVNRDxBq0Z-xwOUFoIcQLYcL3hrsmepIAyVdZI88Bnec130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP127006.RAVNRDxBq0Z-xwOUFoIcQLYcL3hrsmepIAyVdZI88Bnec130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP127006.RAVNRDxBq0Z-xwOUFoIcQLYcL3hrsmepIAyVdZI88Bnec130_provenance.
- NP127006.RAVNRDxBq0Z-xwOUFoIcQLYcL3hrsmepIAyVdZI88Bnec130_assertion wasGeneratedBy ECO_0000203 NP127006.RAVNRDxBq0Z-xwOUFoIcQLYcL3hrsmepIAyVdZI88Bnec130_provenance.
- NP127006.RAVNRDxBq0Z-xwOUFoIcQLYcL3hrsmepIAyVdZI88Bnec130_assertion wasDerivedFrom lhgdn-20090331 NP127006.RAVNRDxBq0Z-xwOUFoIcQLYcL3hrsmepIAyVdZI88Bnec130_provenance.
- NP127006.RAVNRDxBq0Z-xwOUFoIcQLYcL3hrsmepIAyVdZI88Bnec130_assertion SIO_000772 12838518 NP127006.RAVNRDxBq0Z-xwOUFoIcQLYcL3hrsmepIAyVdZI88Bnec130_provenance.
- NP127006.RAVNRDxBq0Z-xwOUFoIcQLYcL3hrsmepIAyVdZI88Bnec130_assertion evidence source_evidence_literature NP127006.RAVNRDxBq0Z-xwOUFoIcQLYcL3hrsmepIAyVdZI88Bnec130_provenance.
- NP127006.RAVNRDxBq0Z-xwOUFoIcQLYcL3hrsmepIAyVdZI88Bnec130_assertion description "[Missense DCX mutations may manifest as non-syndromic mental retardation with cryptogenic epilepsy in female subjects and subcortical band heterotopia (SBH) in boys.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP127006.RAVNRDxBq0Z-xwOUFoIcQLYcL3hrsmepIAyVdZI88Bnec130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP127006.RAVNRDxBq0Z-xwOUFoIcQLYcL3hrsmepIAyVdZI88Bnec130_provenance.