Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1295873.RARVYHd0LIA2zjqSke5fgnhnb2hcIbl3_tjzf6vG2Zpv4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1295873.RARVYHd0LIA2zjqSke5fgnhnb2hcIbl3_tjzf6vG2Zpv4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1295873.RARVYHd0LIA2zjqSke5fgnhnb2hcIbl3_tjzf6vG2Zpv4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1295873.RARVYHd0LIA2zjqSke5fgnhnb2hcIbl3_tjzf6vG2Zpv4130_provenance.
- NP1295873.RARVYHd0LIA2zjqSke5fgnhnb2hcIbl3_tjzf6vG2Zpv4130_assertion description "[Three prevalent single nucleotide polymorphisms (SNPs; rs1412444(LIPA), rs662799(APOA5) and rs964184(ZNF259)) associated with CAD and MI in other ethnic populations, were selected for sequence and association analyses within blood DNA of the Chinese Han population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1295873.RARVYHd0LIA2zjqSke5fgnhnb2hcIbl3_tjzf6vG2Zpv4130_provenance.
- NP1295873.RARVYHd0LIA2zjqSke5fgnhnb2hcIbl3_tjzf6vG2Zpv4130_assertion evidence source_evidence_literature NP1295873.RARVYHd0LIA2zjqSke5fgnhnb2hcIbl3_tjzf6vG2Zpv4130_provenance.
- NP1295873.RARVYHd0LIA2zjqSke5fgnhnb2hcIbl3_tjzf6vG2Zpv4130_assertion SIO_000772 26731984 NP1295873.RARVYHd0LIA2zjqSke5fgnhnb2hcIbl3_tjzf6vG2Zpv4130_provenance.
- NP1295873.RARVYHd0LIA2zjqSke5fgnhnb2hcIbl3_tjzf6vG2Zpv4130_assertion wasDerivedFrom befree-2016 NP1295873.RARVYHd0LIA2zjqSke5fgnhnb2hcIbl3_tjzf6vG2Zpv4130_provenance.
- NP1295873.RARVYHd0LIA2zjqSke5fgnhnb2hcIbl3_tjzf6vG2Zpv4130_assertion wasGeneratedBy ECO_0000203 NP1295873.RARVYHd0LIA2zjqSke5fgnhnb2hcIbl3_tjzf6vG2Zpv4130_provenance.
- befree-2016 importedOn "2016-02-19" NP1295873.RARVYHd0LIA2zjqSke5fgnhnb2hcIbl3_tjzf6vG2Zpv4130_provenance.