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- source_evidence_literature type ECO_0000212 NP99631.RAQELbOR8-fXOres-_qfkBcDxiy8WNy1pqosS17Jl_xh4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP99631.RAQELbOR8-fXOres-_qfkBcDxiy8WNy1pqosS17Jl_xh4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP99631.RAQELbOR8-fXOres-_qfkBcDxiy8WNy1pqosS17Jl_xh4130_provenance.
- NP99631.RAQELbOR8-fXOres-_qfkBcDxiy8WNy1pqosS17Jl_xh4130_assertion description "[We genotyped the following 11 SNPs, from 10 loci, in 641 AAV patients using TaqMan genotyping: rs2476601 in PTPN22, rs1990760 in IFIH1, rs3087243 in CTLA4, rs2069763 in IL2, rs10877012 in CYP27B1, rs2292239 in ERBB3, rs3184504 in SH2B3, rs12708716 in CLEC16A, rs1893217 and rs478582 in PTPN2 and rs763361 in CD226.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP99631.RAQELbOR8-fXOres-_qfkBcDxiy8WNy1pqosS17Jl_xh4130_provenance.
- NP99631.RAQELbOR8-fXOres-_qfkBcDxiy8WNy1pqosS17Jl_xh4130_assertion evidence source_evidence_literature NP99631.RAQELbOR8-fXOres-_qfkBcDxiy8WNy1pqosS17Jl_xh4130_provenance.
- NP99631.RAQELbOR8-fXOres-_qfkBcDxiy8WNy1pqosS17Jl_xh4130_assertion SIO_000772 19951419 NP99631.RAQELbOR8-fXOres-_qfkBcDxiy8WNy1pqosS17Jl_xh4130_provenance.
- NP99631.RAQELbOR8-fXOres-_qfkBcDxiy8WNy1pqosS17Jl_xh4130_assertion wasDerivedFrom gad-20150221 NP99631.RAQELbOR8-fXOres-_qfkBcDxiy8WNy1pqosS17Jl_xh4130_provenance.
- NP99631.RAQELbOR8-fXOres-_qfkBcDxiy8WNy1pqosS17Jl_xh4130_assertion wasGeneratedBy ECO_0000203 NP99631.RAQELbOR8-fXOres-_qfkBcDxiy8WNy1pqosS17Jl_xh4130_provenance.
- gad-20150221 importedOn "2015-02-21" NP99631.RAQELbOR8-fXOres-_qfkBcDxiy8WNy1pqosS17Jl_xh4130_provenance.