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- NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_assertion type Assertion NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_head.
- NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_assertion description "[The celtic coincidence--the frequency and clinical characterisation of hereditary haemochromatosis in patients with coeliac disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_provenance.
- NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_assertion evidence source_evidence_literature NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_provenance.
- NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_assertion SIO_000772 16615226 NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_provenance.
- NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_assertion wasDerivedFrom gad-20150221 NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_provenance.
- NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_assertion wasGeneratedBy ECO_0000203 NP100051.RA84FiELs4yh4J2TrllCko3MQlUshg35x9-H3T-9s78Y4130_provenance.