Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP684175.RAKTMJF9hgXAXCtqPqVvnvQhiG_ew4Vf-E_nUhJtSQ6rQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP684175.RAKTMJF9hgXAXCtqPqVvnvQhiG_ew4Vf-E_nUhJtSQ6rQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP684175.RAKTMJF9hgXAXCtqPqVvnvQhiG_ew4Vf-E_nUhJtSQ6rQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP684175.RAKTMJF9hgXAXCtqPqVvnvQhiG_ew4Vf-E_nUhJtSQ6rQ130_provenance.
- NP684175.RAKTMJF9hgXAXCtqPqVvnvQhiG_ew4Vf-E_nUhJtSQ6rQ130_assertion description "[An A8296G mutation in the MT-TK gene of a patient with epilepsy - a disease-causing mutation or rare polymorphism?]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP684175.RAKTMJF9hgXAXCtqPqVvnvQhiG_ew4Vf-E_nUhJtSQ6rQ130_provenance.
- NP684175.RAKTMJF9hgXAXCtqPqVvnvQhiG_ew4Vf-E_nUhJtSQ6rQ130_assertion evidence source_evidence_literature NP684175.RAKTMJF9hgXAXCtqPqVvnvQhiG_ew4Vf-E_nUhJtSQ6rQ130_provenance.
- NP684175.RAKTMJF9hgXAXCtqPqVvnvQhiG_ew4Vf-E_nUhJtSQ6rQ130_assertion SIO_000772 18651333 NP684175.RAKTMJF9hgXAXCtqPqVvnvQhiG_ew4Vf-E_nUhJtSQ6rQ130_provenance.
- NP684175.RAKTMJF9hgXAXCtqPqVvnvQhiG_ew4Vf-E_nUhJtSQ6rQ130_assertion wasDerivedFrom befree-2016 NP684175.RAKTMJF9hgXAXCtqPqVvnvQhiG_ew4Vf-E_nUhJtSQ6rQ130_provenance.
- NP684175.RAKTMJF9hgXAXCtqPqVvnvQhiG_ew4Vf-E_nUhJtSQ6rQ130_assertion wasGeneratedBy ECO_0000203 NP684175.RAKTMJF9hgXAXCtqPqVvnvQhiG_ew4Vf-E_nUhJtSQ6rQ130_provenance.
- befree-2016 importedOn "2016-02-19" NP684175.RAKTMJF9hgXAXCtqPqVvnvQhiG_ew4Vf-E_nUhJtSQ6rQ130_provenance.