http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg#head http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg#assertion http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg#provenance http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg#assertion http://rdf.disgenet.org/resource/gda/DGNef4b4a50abcebaab704634f17b2fcf94 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/2969 http://rdf.disgenet.org/resource/gda/DGNef4b4a50abcebaab704634f17b2fcf94 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0175702 http://rdf.disgenet.org/resource/gda/DGNef4b4a50abcebaab704634f17b2fcf94 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001121 http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg#provenance http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg#assertion http://purl.org/dc/terms/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. http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/22608712 http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://purl.org/dc/terms/created 2017-10-17T13:13:11+02:00 http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP472213.RAFm5auUTa0nS15pCIyG802TUFYBQIrEPY4IeoGO5PWQg http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0