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- source_evidence_literature type ECO_0000212 NP507935.RAPfM0S2GAV6KEYzuwRyHIuX6bC3aUFAgVuYJ4LyJ3oOw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP507935.RAPfM0S2GAV6KEYzuwRyHIuX6bC3aUFAgVuYJ4LyJ3oOw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP507935.RAPfM0S2GAV6KEYzuwRyHIuX6bC3aUFAgVuYJ4LyJ3oOw130_provenance.
- NP507935.RAPfM0S2GAV6KEYzuwRyHIuX6bC3aUFAgVuYJ4LyJ3oOw130_assertion description "[Based on our data, we speculated that the SNP rs8193037 of IL17A gene is significantly associated with CAD risk in Chinese Han population and the rs8193037 G allele which is associated with increased expression of IL17A in AMI patients may be an independent predictive factor for CAD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP507935.RAPfM0S2GAV6KEYzuwRyHIuX6bC3aUFAgVuYJ4LyJ3oOw130_provenance.
- NP507935.RAPfM0S2GAV6KEYzuwRyHIuX6bC3aUFAgVuYJ4LyJ3oOw130_assertion evidence source_evidence_literature NP507935.RAPfM0S2GAV6KEYzuwRyHIuX6bC3aUFAgVuYJ4LyJ3oOw130_provenance.
- NP507935.RAPfM0S2GAV6KEYzuwRyHIuX6bC3aUFAgVuYJ4LyJ3oOw130_assertion SIO_000772 21062626 NP507935.RAPfM0S2GAV6KEYzuwRyHIuX6bC3aUFAgVuYJ4LyJ3oOw130_provenance.
- NP507935.RAPfM0S2GAV6KEYzuwRyHIuX6bC3aUFAgVuYJ4LyJ3oOw130_assertion wasDerivedFrom befree-20150227 NP507935.RAPfM0S2GAV6KEYzuwRyHIuX6bC3aUFAgVuYJ4LyJ3oOw130_provenance.
- NP507935.RAPfM0S2GAV6KEYzuwRyHIuX6bC3aUFAgVuYJ4LyJ3oOw130_assertion wasGeneratedBy ECO_0000203 NP507935.RAPfM0S2GAV6KEYzuwRyHIuX6bC3aUFAgVuYJ4LyJ3oOw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP507935.RAPfM0S2GAV6KEYzuwRyHIuX6bC3aUFAgVuYJ4LyJ3oOw130_provenance.