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- source_evidence_literature type ECO_0000212 NP300095.RAM1a7JcmS0xsgrV7k7Y8ykZptYEA2vd2F1RHib5RW_CE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP300095.RAM1a7JcmS0xsgrV7k7Y8ykZptYEA2vd2F1RHib5RW_CE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP300095.RAM1a7JcmS0xsgrV7k7Y8ykZptYEA2vd2F1RHib5RW_CE130_provenance.
- NP300095.RAM1a7JcmS0xsgrV7k7Y8ykZptYEA2vd2F1RHib5RW_CE130_assertion description "[Five SNPs achieved 0.004 (the nominal p-value expected by chance), 3 with empirical significant p-values (rs10070190 (CDH9) p�=�1�נ10(-3), rs4825476 (GRIA3) p�=�4�נ10(-4), and rs1074815 (TPH2) p�=�8�נ10(-4)) and 2 additional polymorphisms showing nominal significance (rs2834070 (OLIG2) p�=�2�נ10(-3) and rs11783752 (SCL18A1) p�=�3�נ10(-3)), were found to be related to both AN and OCD.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP300095.RAM1a7JcmS0xsgrV7k7Y8ykZptYEA2vd2F1RHib5RW_CE130_provenance.
- NP300095.RAM1a7JcmS0xsgrV7k7Y8ykZptYEA2vd2F1RHib5RW_CE130_assertion evidence source_evidence_literature NP300095.RAM1a7JcmS0xsgrV7k7Y8ykZptYEA2vd2F1RHib5RW_CE130_provenance.
- NP300095.RAM1a7JcmS0xsgrV7k7Y8ykZptYEA2vd2F1RHib5RW_CE130_assertion SIO_000772 23337130 NP300095.RAM1a7JcmS0xsgrV7k7Y8ykZptYEA2vd2F1RHib5RW_CE130_provenance.
- NP300095.RAM1a7JcmS0xsgrV7k7Y8ykZptYEA2vd2F1RHib5RW_CE130_assertion wasDerivedFrom befree-20150227 NP300095.RAM1a7JcmS0xsgrV7k7Y8ykZptYEA2vd2F1RHib5RW_CE130_provenance.
- NP300095.RAM1a7JcmS0xsgrV7k7Y8ykZptYEA2vd2F1RHib5RW_CE130_assertion wasGeneratedBy ECO_0000203 NP300095.RAM1a7JcmS0xsgrV7k7Y8ykZptYEA2vd2F1RHib5RW_CE130_provenance.
- befree-20150227 importedOn "2015-02-27" NP300095.RAM1a7JcmS0xsgrV7k7Y8ykZptYEA2vd2F1RHib5RW_CE130_provenance.