Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP58979.RA7mSHbY-yvRkZlvnmwuDHThlnDl4OH9YEe277_d0U8hE130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP58979.RA7mSHbY-yvRkZlvnmwuDHThlnDl4OH9YEe277_d0U8hE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP58979.RA7mSHbY-yvRkZlvnmwuDHThlnDl4OH9YEe277_d0U8hE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP58979.RA7mSHbY-yvRkZlvnmwuDHThlnDl4OH9YEe277_d0U8hE130_provenance.
- gad-20150221 importedOn "2015-02-21" NP58979.RA7mSHbY-yvRkZlvnmwuDHThlnDl4OH9YEe277_d0U8hE130_provenance.
- NP58979.RA7mSHbY-yvRkZlvnmwuDHThlnDl4OH9YEe277_d0U8hE130_assertion wasGeneratedBy ECO_0000203 NP58979.RA7mSHbY-yvRkZlvnmwuDHThlnDl4OH9YEe277_d0U8hE130_provenance.
- NP58979.RA7mSHbY-yvRkZlvnmwuDHThlnDl4OH9YEe277_d0U8hE130_assertion wasDerivedFrom gad-20150221 NP58979.RA7mSHbY-yvRkZlvnmwuDHThlnDl4OH9YEe277_d0U8hE130_provenance.
- NP58979.RA7mSHbY-yvRkZlvnmwuDHThlnDl4OH9YEe277_d0U8hE130_assertion SIO_000772 14959997 NP58979.RA7mSHbY-yvRkZlvnmwuDHThlnDl4OH9YEe277_d0U8hE130_provenance.
- NP58979.RA7mSHbY-yvRkZlvnmwuDHThlnDl4OH9YEe277_d0U8hE130_assertion evidence source_evidence_literature NP58979.RA7mSHbY-yvRkZlvnmwuDHThlnDl4OH9YEe277_d0U8hE130_provenance.
- NP58979.RA7mSHbY-yvRkZlvnmwuDHThlnDl4OH9YEe277_d0U8hE130_assertion description "[In summary, we found significant ethnic-specific and gender-based differences in the frequency of the minor allele of the -1131 APOA-V gene promoter polymorphism. Identification of genetic variations among ethnic groups and between genders may have signif]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP58979.RA7mSHbY-yvRkZlvnmwuDHThlnDl4OH9YEe277_d0U8hE130_provenance.