Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP898908.RAk6-mpw2i-jeskGiy79tZ8cVton4swiNrfl30qn0w9vg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP898908.RAk6-mpw2i-jeskGiy79tZ8cVton4swiNrfl30qn0w9vg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP898908.RAk6-mpw2i-jeskGiy79tZ8cVton4swiNrfl30qn0w9vg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP898908.RAk6-mpw2i-jeskGiy79tZ8cVton4swiNrfl30qn0w9vg130_provenance.
- NP898908.RAk6-mpw2i-jeskGiy79tZ8cVton4swiNrfl30qn0w9vg130_assertion description "[Mutations in TNK2 in severe autosomal recessive infantile onset epilepsy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP898908.RAk6-mpw2i-jeskGiy79tZ8cVton4swiNrfl30qn0w9vg130_provenance.
- NP898908.RAk6-mpw2i-jeskGiy79tZ8cVton4swiNrfl30qn0w9vg130_assertion evidence source_evidence_literature NP898908.RAk6-mpw2i-jeskGiy79tZ8cVton4swiNrfl30qn0w9vg130_provenance.
- NP898908.RAk6-mpw2i-jeskGiy79tZ8cVton4swiNrfl30qn0w9vg130_assertion SIO_000772 23686771 NP898908.RAk6-mpw2i-jeskGiy79tZ8cVton4swiNrfl30qn0w9vg130_provenance.
- NP898908.RAk6-mpw2i-jeskGiy79tZ8cVton4swiNrfl30qn0w9vg130_assertion wasDerivedFrom befree-20140225 NP898908.RAk6-mpw2i-jeskGiy79tZ8cVton4swiNrfl30qn0w9vg130_provenance.
- NP898908.RAk6-mpw2i-jeskGiy79tZ8cVton4swiNrfl30qn0w9vg130_assertion wasGeneratedBy ECO_0000203 NP898908.RAk6-mpw2i-jeskGiy79tZ8cVton4swiNrfl30qn0w9vg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP898908.RAk6-mpw2i-jeskGiy79tZ8cVton4swiNrfl30qn0w9vg130_provenance.