Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP584777.RAYhcAm8zzgcwyyGY25a1TbP9Ij2Kx2ROErHCLVYug4_A130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP584777.RAYhcAm8zzgcwyyGY25a1TbP9Ij2Kx2ROErHCLVYug4_A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP584777.RAYhcAm8zzgcwyyGY25a1TbP9Ij2Kx2ROErHCLVYug4_A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP584777.RAYhcAm8zzgcwyyGY25a1TbP9Ij2Kx2ROErHCLVYug4_A130_provenance.
- NP584777.RAYhcAm8zzgcwyyGY25a1TbP9Ij2Kx2ROErHCLVYug4_A130_assertion description "[We demonstrate that DRD2 polymorphisms -141Cdel, 3208G>T, TaqIB; DRD4 -521C>T and DAT1/SLC6A3 -1476T>G are associated with a two- to five-fold increased NSCLC risk.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP584777.RAYhcAm8zzgcwyyGY25a1TbP9Ij2Kx2ROErHCLVYug4_A130_provenance.
- NP584777.RAYhcAm8zzgcwyyGY25a1TbP9Ij2Kx2ROErHCLVYug4_A130_assertion evidence source_evidence_literature NP584777.RAYhcAm8zzgcwyyGY25a1TbP9Ij2Kx2ROErHCLVYug4_A130_provenance.
- NP584777.RAYhcAm8zzgcwyyGY25a1TbP9Ij2Kx2ROErHCLVYug4_A130_assertion SIO_000772 17175058 NP584777.RAYhcAm8zzgcwyyGY25a1TbP9Ij2Kx2ROErHCLVYug4_A130_provenance.
- NP584777.RAYhcAm8zzgcwyyGY25a1TbP9Ij2Kx2ROErHCLVYug4_A130_assertion wasDerivedFrom befree-2016 NP584777.RAYhcAm8zzgcwyyGY25a1TbP9Ij2Kx2ROErHCLVYug4_A130_provenance.
- NP584777.RAYhcAm8zzgcwyyGY25a1TbP9Ij2Kx2ROErHCLVYug4_A130_assertion wasGeneratedBy ECO_0000203 NP584777.RAYhcAm8zzgcwyyGY25a1TbP9Ij2Kx2ROErHCLVYug4_A130_provenance.
- befree-2016 importedOn "2016-02-19" NP584777.RAYhcAm8zzgcwyyGY25a1TbP9Ij2Kx2ROErHCLVYug4_A130_provenance.