Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP265909.RAs-BD1JGxLQrBeexgjIGEqeR3IYopJfQk9H0n4KBfcOA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP265909.RAs-BD1JGxLQrBeexgjIGEqeR3IYopJfQk9H0n4KBfcOA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP265909.RAs-BD1JGxLQrBeexgjIGEqeR3IYopJfQk9H0n4KBfcOA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP265909.RAs-BD1JGxLQrBeexgjIGEqeR3IYopJfQk9H0n4KBfcOA130_provenance.
- NP265909.RAs-BD1JGxLQrBeexgjIGEqeR3IYopJfQk9H0n4KBfcOA130_assertion description "[Mutations of the coding region of DCX were found in all reported pedigrees and in about 50% of sporadic female patients with subcortical band heterotopia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP265909.RAs-BD1JGxLQrBeexgjIGEqeR3IYopJfQk9H0n4KBfcOA130_provenance.
- NP265909.RAs-BD1JGxLQrBeexgjIGEqeR3IYopJfQk9H0n4KBfcOA130_assertion evidence source_evidence_literature NP265909.RAs-BD1JGxLQrBeexgjIGEqeR3IYopJfQk9H0n4KBfcOA130_provenance.
- NP265909.RAs-BD1JGxLQrBeexgjIGEqeR3IYopJfQk9H0n4KBfcOA130_assertion SIO_000772 15921228 NP265909.RAs-BD1JGxLQrBeexgjIGEqeR3IYopJfQk9H0n4KBfcOA130_provenance.
- NP265909.RAs-BD1JGxLQrBeexgjIGEqeR3IYopJfQk9H0n4KBfcOA130_assertion wasDerivedFrom befree-20140225 NP265909.RAs-BD1JGxLQrBeexgjIGEqeR3IYopJfQk9H0n4KBfcOA130_provenance.
- NP265909.RAs-BD1JGxLQrBeexgjIGEqeR3IYopJfQk9H0n4KBfcOA130_assertion wasGeneratedBy ECO_0000203 NP265909.RAs-BD1JGxLQrBeexgjIGEqeR3IYopJfQk9H0n4KBfcOA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP265909.RAs-BD1JGxLQrBeexgjIGEqeR3IYopJfQk9H0n4KBfcOA130_provenance.