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- source_evidence_literature type ECO_0000212 NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_provenance.
- NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_assertion description "[Hp2-2 was less frequent in patients than in controls (P = 0.0023), but patients having this phenotype were at an increased risk for severe malabsorption (OR 2.21, 95% CI 1.60-3.07) and accounted for 45.3% of all malabsorption cases.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_provenance.
- NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_assertion evidence source_evidence_literature NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_provenance.
- NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_assertion SIO_000772 18258668 NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_provenance.
- NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_assertion wasDerivedFrom befree-20150227 NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_provenance.
- NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_assertion wasGeneratedBy ECO_0000203 NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_provenance.