http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM#head http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM#assertion http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM#provenance http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM#assertion http://rdf.disgenet.org/resource/gda/DGNc6064796d2e3dd4cc452fbd36a207553 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/6657 http://rdf.disgenet.org/resource/gda/DGNc6064796d2e3dd4cc452fbd36a207553 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0014556 http://rdf.disgenet.org/resource/gda/DGNc6064796d2e3dd4cc452fbd36a207553 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM#provenance http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM#assertion http://purl.org/dc/terms/description [However, although mutation of SOX2 in humans causes hippocampal malformation, SOX2 mutation or variation is unlikely to contribute commonly to mesial temporal lobe epilepsy or its structural (hippocampal sclerosis) or historic (febrile seizures) associations in humans.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM#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/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/16529618 http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM#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/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM http://purl.org/dc/terms/created 2017-10-17T13:16:23+02:00 http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP972492.RAChpvQF1eWbC5ltbz2m7a3QzhfDKgQfH-N4-_2BhvXbM 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