Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP569686.RAMotnNqu9nMShSKmsEDpi9jSRkoCnk9x1zs1_Ufzor6g130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP569686.RAMotnNqu9nMShSKmsEDpi9jSRkoCnk9x1zs1_Ufzor6g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP569686.RAMotnNqu9nMShSKmsEDpi9jSRkoCnk9x1zs1_Ufzor6g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP569686.RAMotnNqu9nMShSKmsEDpi9jSRkoCnk9x1zs1_Ufzor6g130_provenance.
- NP569686.RAMotnNqu9nMShSKmsEDpi9jSRkoCnk9x1zs1_Ufzor6g130_assertion description "[The haplotype (GGT) consisting of all three risk alleles was significantly overrepresented (87.5%) in patients with PEX.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP569686.RAMotnNqu9nMShSKmsEDpi9jSRkoCnk9x1zs1_Ufzor6g130_provenance.
- NP569686.RAMotnNqu9nMShSKmsEDpi9jSRkoCnk9x1zs1_Ufzor6g130_assertion evidence source_evidence_literature NP569686.RAMotnNqu9nMShSKmsEDpi9jSRkoCnk9x1zs1_Ufzor6g130_provenance.
- NP569686.RAMotnNqu9nMShSKmsEDpi9jSRkoCnk9x1zs1_Ufzor6g130_assertion SIO_000772 21272281 NP569686.RAMotnNqu9nMShSKmsEDpi9jSRkoCnk9x1zs1_Ufzor6g130_provenance.
- NP569686.RAMotnNqu9nMShSKmsEDpi9jSRkoCnk9x1zs1_Ufzor6g130_assertion wasDerivedFrom befree-20140225 NP569686.RAMotnNqu9nMShSKmsEDpi9jSRkoCnk9x1zs1_Ufzor6g130_provenance.
- NP569686.RAMotnNqu9nMShSKmsEDpi9jSRkoCnk9x1zs1_Ufzor6g130_assertion wasGeneratedBy ECO_0000203 NP569686.RAMotnNqu9nMShSKmsEDpi9jSRkoCnk9x1zs1_Ufzor6g130_provenance.
- befree-20140225 importedOn "2014-02-25" NP569686.RAMotnNqu9nMShSKmsEDpi9jSRkoCnk9x1zs1_Ufzor6g130_provenance.