Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP471751.RAPB8MyQJr3vKRbkk04Dc2oE7XJY9ErENArK4Gn5ZwflE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP471751.RAPB8MyQJr3vKRbkk04Dc2oE7XJY9ErENArK4Gn5ZwflE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP471751.RAPB8MyQJr3vKRbkk04Dc2oE7XJY9ErENArK4Gn5ZwflE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP471751.RAPB8MyQJr3vKRbkk04Dc2oE7XJY9ErENArK4Gn5ZwflE130_provenance.
- NP471751.RAPB8MyQJr3vKRbkk04Dc2oE7XJY9ErENArK4Gn5ZwflE130_assertion description "[ARX mutations are associated with various forms of epilepsy, developmental delay, and ambiguous genitalia in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP471751.RAPB8MyQJr3vKRbkk04Dc2oE7XJY9ErENArK4Gn5ZwflE130_provenance.
- NP471751.RAPB8MyQJr3vKRbkk04Dc2oE7XJY9ErENArK4Gn5ZwflE130_assertion evidence source_evidence_literature NP471751.RAPB8MyQJr3vKRbkk04Dc2oE7XJY9ErENArK4Gn5ZwflE130_provenance.
- NP471751.RAPB8MyQJr3vKRbkk04Dc2oE7XJY9ErENArK4Gn5ZwflE130_assertion SIO_000772 21426321 NP471751.RAPB8MyQJr3vKRbkk04Dc2oE7XJY9ErENArK4Gn5ZwflE130_provenance.
- NP471751.RAPB8MyQJr3vKRbkk04Dc2oE7XJY9ErENArK4Gn5ZwflE130_assertion wasDerivedFrom befree-20140225 NP471751.RAPB8MyQJr3vKRbkk04Dc2oE7XJY9ErENArK4Gn5ZwflE130_provenance.
- NP471751.RAPB8MyQJr3vKRbkk04Dc2oE7XJY9ErENArK4Gn5ZwflE130_assertion wasGeneratedBy ECO_0000203 NP471751.RAPB8MyQJr3vKRbkk04Dc2oE7XJY9ErENArK4Gn5ZwflE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP471751.RAPB8MyQJr3vKRbkk04Dc2oE7XJY9ErENArK4Gn5ZwflE130_provenance.