Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1246232.RAq7OU0JcmGLJh6kYfb05PHFwSnXIBLigDyjkxhqZ0a64130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1246232.RAq7OU0JcmGLJh6kYfb05PHFwSnXIBLigDyjkxhqZ0a64130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1246232.RAq7OU0JcmGLJh6kYfb05PHFwSnXIBLigDyjkxhqZ0a64130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1246232.RAq7OU0JcmGLJh6kYfb05PHFwSnXIBLigDyjkxhqZ0a64130_provenance.
- NP1246232.RAq7OU0JcmGLJh6kYfb05PHFwSnXIBLigDyjkxhqZ0a64130_assertion description "[These findings suggested that the TC genotype of SNP rs3999941 and AC genotype of the new SNP c.657A>C in the TBX20 gene may be risk factors for CHD and thus screening of these SNPs may have some implications in the prevention and treatment of CHD in Han Chinese children.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1246232.RAq7OU0JcmGLJh6kYfb05PHFwSnXIBLigDyjkxhqZ0a64130_provenance.
- NP1246232.RAq7OU0JcmGLJh6kYfb05PHFwSnXIBLigDyjkxhqZ0a64130_assertion evidence source_evidence_literature NP1246232.RAq7OU0JcmGLJh6kYfb05PHFwSnXIBLigDyjkxhqZ0a64130_provenance.
- NP1246232.RAq7OU0JcmGLJh6kYfb05PHFwSnXIBLigDyjkxhqZ0a64130_assertion SIO_000772 25487630 NP1246232.RAq7OU0JcmGLJh6kYfb05PHFwSnXIBLigDyjkxhqZ0a64130_provenance.
- NP1246232.RAq7OU0JcmGLJh6kYfb05PHFwSnXIBLigDyjkxhqZ0a64130_assertion wasDerivedFrom befree-2016 NP1246232.RAq7OU0JcmGLJh6kYfb05PHFwSnXIBLigDyjkxhqZ0a64130_provenance.
- NP1246232.RAq7OU0JcmGLJh6kYfb05PHFwSnXIBLigDyjkxhqZ0a64130_assertion wasGeneratedBy ECO_0000203 NP1246232.RAq7OU0JcmGLJh6kYfb05PHFwSnXIBLigDyjkxhqZ0a64130_provenance.
- befree-2016 importedOn "2016-02-19" NP1246232.RAq7OU0JcmGLJh6kYfb05PHFwSnXIBLigDyjkxhqZ0a64130_provenance.