Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_provenance.
- NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_assertion description "[Although contribution of CLIP2 to the phenotype cannot be excluded when it is deleted in combination with other genes, our results support the hypothesis that GTF2IRD1 and GTF2I are the main genes causing the cognitive defects associated with Williams-Beuren syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_provenance.
- NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_assertion evidence source_evidence_literature NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_provenance.
- NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_assertion SIO_000772 22608712 NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_provenance.
- NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_assertion wasDerivedFrom befree-2016 NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_provenance.
- NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_assertion wasGeneratedBy ECO_0000203 NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_provenance.
- befree-2016 importedOn "2016-02-19" NP983483.RAF5tz1OqaKT5xeTmAKTlu_UohO-agSb5dm5w-yfp2BmU130_provenance.