Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP978098.RA027BwVumPMF2Nb4lG3CSYq_a2qWsiljLF-DNbqwHt2w130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP978098.RA027BwVumPMF2Nb4lG3CSYq_a2qWsiljLF-DNbqwHt2w130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP978098.RA027BwVumPMF2Nb4lG3CSYq_a2qWsiljLF-DNbqwHt2w130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP978098.RA027BwVumPMF2Nb4lG3CSYq_a2qWsiljLF-DNbqwHt2w130_provenance.
- NP978098.RA027BwVumPMF2Nb4lG3CSYq_a2qWsiljLF-DNbqwHt2w130_assertion description "[Mutations in the Aristaless-related homeobox gene, ARX, have been a cause of X-linked mental retardation (XLMR) and are responsible for a vast phenotypic spectrum including syndromic and non-syndromic forms of mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP978098.RA027BwVumPMF2Nb4lG3CSYq_a2qWsiljLF-DNbqwHt2w130_provenance.
- NP978098.RA027BwVumPMF2Nb4lG3CSYq_a2qWsiljLF-DNbqwHt2w130_assertion evidence source_evidence_literature NP978098.RA027BwVumPMF2Nb4lG3CSYq_a2qWsiljLF-DNbqwHt2w130_provenance.
- NP978098.RA027BwVumPMF2Nb4lG3CSYq_a2qWsiljLF-DNbqwHt2w130_assertion SIO_000772 17613295 NP978098.RA027BwVumPMF2Nb4lG3CSYq_a2qWsiljLF-DNbqwHt2w130_provenance.
- NP978098.RA027BwVumPMF2Nb4lG3CSYq_a2qWsiljLF-DNbqwHt2w130_assertion wasDerivedFrom befree-20150227 NP978098.RA027BwVumPMF2Nb4lG3CSYq_a2qWsiljLF-DNbqwHt2w130_provenance.
- NP978098.RA027BwVumPMF2Nb4lG3CSYq_a2qWsiljLF-DNbqwHt2w130_assertion wasGeneratedBy ECO_0000203 NP978098.RA027BwVumPMF2Nb4lG3CSYq_a2qWsiljLF-DNbqwHt2w130_provenance.
- befree-20150227 importedOn "2015-02-27" NP978098.RA027BwVumPMF2Nb4lG3CSYq_a2qWsiljLF-DNbqwHt2w130_provenance.