Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP243665.RATLfzKLH3yA1vXDHIRmeE4j0K_-KqY5hNDv0PcJMBYTY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP243665.RATLfzKLH3yA1vXDHIRmeE4j0K_-KqY5hNDv0PcJMBYTY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP243665.RATLfzKLH3yA1vXDHIRmeE4j0K_-KqY5hNDv0PcJMBYTY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP243665.RATLfzKLH3yA1vXDHIRmeE4j0K_-KqY5hNDv0PcJMBYTY130_provenance.
- NP243665.RATLfzKLH3yA1vXDHIRmeE4j0K_-KqY5hNDv0PcJMBYTY130_assertion description "[However, there is no evidence that APOA5 S19W, -12,238T > C, APOA4 T347S and APCC3 -482C > T SNPs are major risk factors of CHD in French men.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP243665.RATLfzKLH3yA1vXDHIRmeE4j0K_-KqY5hNDv0PcJMBYTY130_provenance.
- NP243665.RATLfzKLH3yA1vXDHIRmeE4j0K_-KqY5hNDv0PcJMBYTY130_assertion evidence source_evidence_literature NP243665.RATLfzKLH3yA1vXDHIRmeE4j0K_-KqY5hNDv0PcJMBYTY130_provenance.
- NP243665.RATLfzKLH3yA1vXDHIRmeE4j0K_-KqY5hNDv0PcJMBYTY130_assertion SIO_000772 16321685 NP243665.RATLfzKLH3yA1vXDHIRmeE4j0K_-KqY5hNDv0PcJMBYTY130_provenance.
- NP243665.RATLfzKLH3yA1vXDHIRmeE4j0K_-KqY5hNDv0PcJMBYTY130_assertion wasDerivedFrom befree-20150227 NP243665.RATLfzKLH3yA1vXDHIRmeE4j0K_-KqY5hNDv0PcJMBYTY130_provenance.
- NP243665.RATLfzKLH3yA1vXDHIRmeE4j0K_-KqY5hNDv0PcJMBYTY130_assertion wasGeneratedBy ECO_0000203 NP243665.RATLfzKLH3yA1vXDHIRmeE4j0K_-KqY5hNDv0PcJMBYTY130_provenance.
- befree-20150227 importedOn "2015-02-27" NP243665.RATLfzKLH3yA1vXDHIRmeE4j0K_-KqY5hNDv0PcJMBYTY130_provenance.