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- source_evidence_literature type ECO_0000212 NP1152956.RAXQ_Rj6A5FPwd4y89le7S86q9irC3j7nM6sYfTjnb1rg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1152956.RAXQ_Rj6A5FPwd4y89le7S86q9irC3j7nM6sYfTjnb1rg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1152956.RAXQ_Rj6A5FPwd4y89le7S86q9irC3j7nM6sYfTjnb1rg130_provenance.
- NP1152956.RAXQ_Rj6A5FPwd4y89le7S86q9irC3j7nM6sYfTjnb1rg130_assertion description "[Our findings provide empirical evidence that SELE genetic polymorphisms may contribute to the pathogenesis of CHD and MI, especially among Asians and Caucasians.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1152956.RAXQ_Rj6A5FPwd4y89le7S86q9irC3j7nM6sYfTjnb1rg130_provenance.
- NP1152956.RAXQ_Rj6A5FPwd4y89le7S86q9irC3j7nM6sYfTjnb1rg130_assertion evidence source_evidence_literature NP1152956.RAXQ_Rj6A5FPwd4y89le7S86q9irC3j7nM6sYfTjnb1rg130_provenance.
- NP1152956.RAXQ_Rj6A5FPwd4y89le7S86q9irC3j7nM6sYfTjnb1rg130_assertion SIO_000772 24504449 NP1152956.RAXQ_Rj6A5FPwd4y89le7S86q9irC3j7nM6sYfTjnb1rg130_provenance.
- NP1152956.RAXQ_Rj6A5FPwd4y89le7S86q9irC3j7nM6sYfTjnb1rg130_assertion wasDerivedFrom befree-2016 NP1152956.RAXQ_Rj6A5FPwd4y89le7S86q9irC3j7nM6sYfTjnb1rg130_provenance.
- NP1152956.RAXQ_Rj6A5FPwd4y89le7S86q9irC3j7nM6sYfTjnb1rg130_assertion wasGeneratedBy ECO_0000203 NP1152956.RAXQ_Rj6A5FPwd4y89le7S86q9irC3j7nM6sYfTjnb1rg130_provenance.
- befree-2016 importedOn "2016-02-19" NP1152956.RAXQ_Rj6A5FPwd4y89le7S86q9irC3j7nM6sYfTjnb1rg130_provenance.