Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_assertion> ?p ?o ?g. }
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- NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_assertion type Assertion NP983667.RAnGm_u3EVEvTbmjxsPtNsALL4hB2Q-75tc6Exi1HFF5o130_head.
- 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.