Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP263004.RAXxKcwOA8hVSRe2sLqMaGL0ILKbpMKp-fQdua9F8TUic130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP263004.RAXxKcwOA8hVSRe2sLqMaGL0ILKbpMKp-fQdua9F8TUic130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP263004.RAXxKcwOA8hVSRe2sLqMaGL0ILKbpMKp-fQdua9F8TUic130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP263004.RAXxKcwOA8hVSRe2sLqMaGL0ILKbpMKp-fQdua9F8TUic130_provenance.
- NP263004.RAXxKcwOA8hVSRe2sLqMaGL0ILKbpMKp-fQdua9F8TUic130_assertion description "[ZNF261 at Xq13.1 is disrupted by a t(X;13)(q13.1;q32) rearrangement in a mentally retarded patient and is a candidate gene for nonspecific X-linked mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP263004.RAXxKcwOA8hVSRe2sLqMaGL0ILKbpMKp-fQdua9F8TUic130_provenance.
- NP263004.RAXxKcwOA8hVSRe2sLqMaGL0ILKbpMKp-fQdua9F8TUic130_assertion evidence source_evidence_literature NP263004.RAXxKcwOA8hVSRe2sLqMaGL0ILKbpMKp-fQdua9F8TUic130_provenance.
- NP263004.RAXxKcwOA8hVSRe2sLqMaGL0ILKbpMKp-fQdua9F8TUic130_assertion SIO_000772 10486218 NP263004.RAXxKcwOA8hVSRe2sLqMaGL0ILKbpMKp-fQdua9F8TUic130_provenance.
- NP263004.RAXxKcwOA8hVSRe2sLqMaGL0ILKbpMKp-fQdua9F8TUic130_assertion wasDerivedFrom befree-2016 NP263004.RAXxKcwOA8hVSRe2sLqMaGL0ILKbpMKp-fQdua9F8TUic130_provenance.
- NP263004.RAXxKcwOA8hVSRe2sLqMaGL0ILKbpMKp-fQdua9F8TUic130_assertion wasGeneratedBy ECO_0000203 NP263004.RAXxKcwOA8hVSRe2sLqMaGL0ILKbpMKp-fQdua9F8TUic130_provenance.
- befree-2016 importedOn "2016-02-19" NP263004.RAXxKcwOA8hVSRe2sLqMaGL0ILKbpMKp-fQdua9F8TUic130_provenance.