Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP316681.RA0Hb2dCC_kiPBERD8k6dTPsJS_1jcjGMDuSnmSxHyltA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP316681.RA0Hb2dCC_kiPBERD8k6dTPsJS_1jcjGMDuSnmSxHyltA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP316681.RA0Hb2dCC_kiPBERD8k6dTPsJS_1jcjGMDuSnmSxHyltA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP316681.RA0Hb2dCC_kiPBERD8k6dTPsJS_1jcjGMDuSnmSxHyltA130_provenance.
- NP316681.RA0Hb2dCC_kiPBERD8k6dTPsJS_1jcjGMDuSnmSxHyltA130_assertion description "[In our analyses of more than 536 cases of clinically undiagnosed multiple congenital anomalies and mental retardation (MR) by microarray-based comparative genomic hybridization, we detected two non-consanguineous unrelated patients with microdeletions at 10p11.23-p12.1, which overlapped for 957 kb, including four protein-coding genes: ARMC4, MPP7, WAC and BAMBI.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP316681.RA0Hb2dCC_kiPBERD8k6dTPsJS_1jcjGMDuSnmSxHyltA130_provenance.
- NP316681.RA0Hb2dCC_kiPBERD8k6dTPsJS_1jcjGMDuSnmSxHyltA130_assertion evidence source_evidence_literature NP316681.RA0Hb2dCC_kiPBERD8k6dTPsJS_1jcjGMDuSnmSxHyltA130_provenance.
- NP316681.RA0Hb2dCC_kiPBERD8k6dTPsJS_1jcjGMDuSnmSxHyltA130_assertion SIO_000772 22258158 NP316681.RA0Hb2dCC_kiPBERD8k6dTPsJS_1jcjGMDuSnmSxHyltA130_provenance.
- NP316681.RA0Hb2dCC_kiPBERD8k6dTPsJS_1jcjGMDuSnmSxHyltA130_assertion wasDerivedFrom befree-20140225 NP316681.RA0Hb2dCC_kiPBERD8k6dTPsJS_1jcjGMDuSnmSxHyltA130_provenance.
- NP316681.RA0Hb2dCC_kiPBERD8k6dTPsJS_1jcjGMDuSnmSxHyltA130_assertion wasGeneratedBy ECO_0000203 NP316681.RA0Hb2dCC_kiPBERD8k6dTPsJS_1jcjGMDuSnmSxHyltA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP316681.RA0Hb2dCC_kiPBERD8k6dTPsJS_1jcjGMDuSnmSxHyltA130_provenance.