Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP867499.RA6X0d1hzg2_CzYV77wLG2RI7IRhyXFsyhTlb1mtzBVac130_assertion> ?p ?o ?g. }
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- NP867499.RA6X0d1hzg2_CzYV77wLG2RI7IRhyXFsyhTlb1mtzBVac130_assertion type Assertion NP867499.RA6X0d1hzg2_CzYV77wLG2RI7IRhyXFsyhTlb1mtzBVac130_head.
- NP867499.RA6X0d1hzg2_CzYV77wLG2RI7IRhyXFsyhTlb1mtzBVac130_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." NP867499.RA6X0d1hzg2_CzYV77wLG2RI7IRhyXFsyhTlb1mtzBVac130_provenance.
- NP867499.RA6X0d1hzg2_CzYV77wLG2RI7IRhyXFsyhTlb1mtzBVac130_assertion evidence source_evidence_literature NP867499.RA6X0d1hzg2_CzYV77wLG2RI7IRhyXFsyhTlb1mtzBVac130_provenance.
- NP867499.RA6X0d1hzg2_CzYV77wLG2RI7IRhyXFsyhTlb1mtzBVac130_assertion SIO_000772 21264219 NP867499.RA6X0d1hzg2_CzYV77wLG2RI7IRhyXFsyhTlb1mtzBVac130_provenance.
- NP867499.RA6X0d1hzg2_CzYV77wLG2RI7IRhyXFsyhTlb1mtzBVac130_assertion wasDerivedFrom befree-2016 NP867499.RA6X0d1hzg2_CzYV77wLG2RI7IRhyXFsyhTlb1mtzBVac130_provenance.
- NP867499.RA6X0d1hzg2_CzYV77wLG2RI7IRhyXFsyhTlb1mtzBVac130_assertion wasGeneratedBy ECO_0000203 NP867499.RA6X0d1hzg2_CzYV77wLG2RI7IRhyXFsyhTlb1mtzBVac130_provenance.