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- source_evidence_literature type ECO_0000212 NP641456.RAqnNywZeLjcfWhl1SwbOqpXp1lXgpDdW4JO-ymY1cSug130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP641456.RAqnNywZeLjcfWhl1SwbOqpXp1lXgpDdW4JO-ymY1cSug130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP641456.RAqnNywZeLjcfWhl1SwbOqpXp1lXgpDdW4JO-ymY1cSug130_provenance.
- NP641456.RAqnNywZeLjcfWhl1SwbOqpXp1lXgpDdW4JO-ymY1cSug130_assertion description "[Epilepsy as part of the phenotype associated with ATP1A2 mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP641456.RAqnNywZeLjcfWhl1SwbOqpXp1lXgpDdW4JO-ymY1cSug130_provenance.
- NP641456.RAqnNywZeLjcfWhl1SwbOqpXp1lXgpDdW4JO-ymY1cSug130_assertion evidence source_evidence_literature NP641456.RAqnNywZeLjcfWhl1SwbOqpXp1lXgpDdW4JO-ymY1cSug130_provenance.
- NP641456.RAqnNywZeLjcfWhl1SwbOqpXp1lXgpDdW4JO-ymY1cSug130_assertion SIO_000772 18028407 NP641456.RAqnNywZeLjcfWhl1SwbOqpXp1lXgpDdW4JO-ymY1cSug130_provenance.
- NP641456.RAqnNywZeLjcfWhl1SwbOqpXp1lXgpDdW4JO-ymY1cSug130_assertion wasDerivedFrom befree-2016 NP641456.RAqnNywZeLjcfWhl1SwbOqpXp1lXgpDdW4JO-ymY1cSug130_provenance.
- NP641456.RAqnNywZeLjcfWhl1SwbOqpXp1lXgpDdW4JO-ymY1cSug130_assertion wasGeneratedBy ECO_0000203 NP641456.RAqnNywZeLjcfWhl1SwbOqpXp1lXgpDdW4JO-ymY1cSug130_provenance.
- befree-2016 importedOn "2016-02-19" NP641456.RAqnNywZeLjcfWhl1SwbOqpXp1lXgpDdW4JO-ymY1cSug130_provenance.