Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1139724.RAVvFF-QMfQnE_1rwvgBITkvjvfKgxB0_-3La9rQG5FiY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1139724.RAVvFF-QMfQnE_1rwvgBITkvjvfKgxB0_-3La9rQG5FiY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1139724.RAVvFF-QMfQnE_1rwvgBITkvjvfKgxB0_-3La9rQG5FiY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1139724.RAVvFF-QMfQnE_1rwvgBITkvjvfKgxB0_-3La9rQG5FiY130_provenance.
- NP1139724.RAVvFF-QMfQnE_1rwvgBITkvjvfKgxB0_-3La9rQG5FiY130_assertion description "[The tumour suppressor gene WWOX is mutated in autosomal recessive cerebellar ataxia with epilepsy and mental retardation.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1139724.RAVvFF-QMfQnE_1rwvgBITkvjvfKgxB0_-3La9rQG5FiY130_provenance.
- NP1139724.RAVvFF-QMfQnE_1rwvgBITkvjvfKgxB0_-3La9rQG5FiY130_assertion evidence source_evidence_literature NP1139724.RAVvFF-QMfQnE_1rwvgBITkvjvfKgxB0_-3La9rQG5FiY130_provenance.
- NP1139724.RAVvFF-QMfQnE_1rwvgBITkvjvfKgxB0_-3La9rQG5FiY130_assertion SIO_000772 24369382 NP1139724.RAVvFF-QMfQnE_1rwvgBITkvjvfKgxB0_-3La9rQG5FiY130_provenance.
- NP1139724.RAVvFF-QMfQnE_1rwvgBITkvjvfKgxB0_-3La9rQG5FiY130_assertion wasDerivedFrom befree-2016 NP1139724.RAVvFF-QMfQnE_1rwvgBITkvjvfKgxB0_-3La9rQG5FiY130_provenance.
- NP1139724.RAVvFF-QMfQnE_1rwvgBITkvjvfKgxB0_-3La9rQG5FiY130_assertion wasGeneratedBy ECO_0000203 NP1139724.RAVvFF-QMfQnE_1rwvgBITkvjvfKgxB0_-3La9rQG5FiY130_provenance.
- befree-2016 importedOn "2016-02-19" NP1139724.RAVvFF-QMfQnE_1rwvgBITkvjvfKgxB0_-3La9rQG5FiY130_provenance.