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- source_evidence_literature type ECO_0000212 NP835138.RAK2i-vFz8_eVNyCiL4jsIcE6UtiQPSRm_ya3MliRkdr0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP835138.RAK2i-vFz8_eVNyCiL4jsIcE6UtiQPSRm_ya3MliRkdr0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP835138.RAK2i-vFz8_eVNyCiL4jsIcE6UtiQPSRm_ya3MliRkdr0130_provenance.
- NP835138.RAK2i-vFz8_eVNyCiL4jsIcE6UtiQPSRm_ya3MliRkdr0130_assertion description "[GJB2 mutation was the most common factor causing NSHL, with a mean frequency of 18.17% in the Iranian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP835138.RAK2i-vFz8_eVNyCiL4jsIcE6UtiQPSRm_ya3MliRkdr0130_provenance.
- NP835138.RAK2i-vFz8_eVNyCiL4jsIcE6UtiQPSRm_ya3MliRkdr0130_assertion evidence source_evidence_literature NP835138.RAK2i-vFz8_eVNyCiL4jsIcE6UtiQPSRm_ya3MliRkdr0130_provenance.
- NP835138.RAK2i-vFz8_eVNyCiL4jsIcE6UtiQPSRm_ya3MliRkdr0130_assertion SIO_000772 20739942 NP835138.RAK2i-vFz8_eVNyCiL4jsIcE6UtiQPSRm_ya3MliRkdr0130_provenance.
- NP835138.RAK2i-vFz8_eVNyCiL4jsIcE6UtiQPSRm_ya3MliRkdr0130_assertion wasDerivedFrom befree-2016 NP835138.RAK2i-vFz8_eVNyCiL4jsIcE6UtiQPSRm_ya3MliRkdr0130_provenance.
- NP835138.RAK2i-vFz8_eVNyCiL4jsIcE6UtiQPSRm_ya3MliRkdr0130_assertion wasGeneratedBy ECO_0000203 NP835138.RAK2i-vFz8_eVNyCiL4jsIcE6UtiQPSRm_ya3MliRkdr0130_provenance.
- befree-2016 importedOn "2016-02-19" NP835138.RAK2i-vFz8_eVNyCiL4jsIcE6UtiQPSRm_ya3MliRkdr0130_provenance.