Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_provenance.
- befree-20150227 importedOn "2015-02-27" NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_provenance.
- NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_assertion wasGeneratedBy ECO_0000203 NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_provenance.
- NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_assertion wasDerivedFrom befree-20150227 NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_provenance.
- NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_assertion SIO_000772 23429546 NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_provenance.
- NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_assertion evidence source_evidence_literature NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_provenance.
- NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_assertion description "[A genome-wide association study in idiopathic generalized epilepsy revealed the first common risk variants for human seizure disorders including variants in VRK2, PNPO and SCN1A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916814.RAi6_dhNvfFjDpQTx0S-wIqkvdAsXkxMncMXug9GBta8I130_provenance.