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- source_evidence_literature type ECO_0000212 NP916142.RAhXlcbd52dHS5jMfEDXFXdhJner-718AVHplt2N2oCdo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP916142.RAhXlcbd52dHS5jMfEDXFXdhJner-718AVHplt2N2oCdo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP916142.RAhXlcbd52dHS5jMfEDXFXdhJner-718AVHplt2N2oCdo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP916142.RAhXlcbd52dHS5jMfEDXFXdhJner-718AVHplt2N2oCdo130_provenance.
- NP916142.RAhXlcbd52dHS5jMfEDXFXdhJner-718AVHplt2N2oCdo130_assertion wasGeneratedBy ECO_0000203 NP916142.RAhXlcbd52dHS5jMfEDXFXdhJner-718AVHplt2N2oCdo130_provenance.
- NP916142.RAhXlcbd52dHS5jMfEDXFXdhJner-718AVHplt2N2oCdo130_assertion wasDerivedFrom befree-20150227 NP916142.RAhXlcbd52dHS5jMfEDXFXdhJner-718AVHplt2N2oCdo130_provenance.
- NP916142.RAhXlcbd52dHS5jMfEDXFXdhJner-718AVHplt2N2oCdo130_assertion SIO_000772 19491842 NP916142.RAhXlcbd52dHS5jMfEDXFXdhJner-718AVHplt2N2oCdo130_provenance.
- NP916142.RAhXlcbd52dHS5jMfEDXFXdhJner-718AVHplt2N2oCdo130_assertion evidence source_evidence_literature NP916142.RAhXlcbd52dHS5jMfEDXFXdhJner-718AVHplt2N2oCdo130_provenance.
- NP916142.RAhXlcbd52dHS5jMfEDXFXdhJner-718AVHplt2N2oCdo130_assertion description "[In conclusion, our results confirm the ATG16L1 rs2241880 and IRGM rs13361189 and rs4958847 polymorphisms as important markers for CD susceptibility and indicate that these variants are also associated with UC.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP916142.RAhXlcbd52dHS5jMfEDXFXdhJner-718AVHplt2N2oCdo130_provenance.