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- source_evidence_literature type ECO_0000212 NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_provenance.
- NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_assertion description "[A mutation in the POU4F3 gene (BRN-3.1, BRN3C) is responsible for DFNA15 (MIM 602459), autosomal-dominant nonsyndromic hearing loss.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_provenance.
- NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_assertion evidence source_evidence_literature NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_provenance.
- NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_assertion SIO_000772 14585957 NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_provenance.
- NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_assertion wasDerivedFrom befree-2016 NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_provenance.
- NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_assertion wasGeneratedBy ECO_0000203 NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_provenance.
- befree-2016 importedOn "2016-02-19" NP418722.RA7ECDsAB42sHcQaRPVgd5GJgeKD1csFehYR2cU2uxEvg130_provenance.