Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP441819.RAeSSrSIJwEtA_Go7LnkbVnjVm_WhKxWf-ttoKko-0_cU130_assertion> ?p ?o ?g. }
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- NP441819.RAeSSrSIJwEtA_Go7LnkbVnjVm_WhKxWf-ttoKko-0_cU130_assertion type Assertion NP441819.RAeSSrSIJwEtA_Go7LnkbVnjVm_WhKxWf-ttoKko-0_cU130_head.
- NP441819.RAeSSrSIJwEtA_Go7LnkbVnjVm_WhKxWf-ttoKko-0_cU130_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." NP441819.RAeSSrSIJwEtA_Go7LnkbVnjVm_WhKxWf-ttoKko-0_cU130_provenance.
- NP441819.RAeSSrSIJwEtA_Go7LnkbVnjVm_WhKxWf-ttoKko-0_cU130_assertion evidence source_evidence_literature NP441819.RAeSSrSIJwEtA_Go7LnkbVnjVm_WhKxWf-ttoKko-0_cU130_provenance.
- NP441819.RAeSSrSIJwEtA_Go7LnkbVnjVm_WhKxWf-ttoKko-0_cU130_assertion SIO_000772 22608712 NP441819.RAeSSrSIJwEtA_Go7LnkbVnjVm_WhKxWf-ttoKko-0_cU130_provenance.
- NP441819.RAeSSrSIJwEtA_Go7LnkbVnjVm_WhKxWf-ttoKko-0_cU130_assertion wasDerivedFrom befree-20150227 NP441819.RAeSSrSIJwEtA_Go7LnkbVnjVm_WhKxWf-ttoKko-0_cU130_provenance.
- NP441819.RAeSSrSIJwEtA_Go7LnkbVnjVm_WhKxWf-ttoKko-0_cU130_assertion wasGeneratedBy ECO_0000203 NP441819.RAeSSrSIJwEtA_Go7LnkbVnjVm_WhKxWf-ttoKko-0_cU130_provenance.