Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_provenance.
- NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_assertion description "[Examination of published literature revealed point mutations in DIA1R are associated with X-linked mental retardation (XLMR) and DIA1R deletion is associated with syndromes with ASD-like traits and/or XLMR.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_provenance.
- NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_assertion evidence source_evidence_literature NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_provenance.
- NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_assertion SIO_000772 21264219 NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_provenance.
- NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_assertion wasDerivedFrom befree-20140225 NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_provenance.
- NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_assertion wasGeneratedBy ECO_0000203 NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_provenance.
- befree-20140225 importedOn "2014-02-25" NP877777.RA9FEux6i4eCv2H70phqlD4rmgRXuEXm6-ubAMuYxaQ-E130_provenance.