Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP198789.RAMXn2U7O_lVcQzhAtkeu9rkO56H_U5opkRC3UDMDyrhk130_assertion> ?p ?o ?g. }
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- NP198789.RAMXn2U7O_lVcQzhAtkeu9rkO56H_U5opkRC3UDMDyrhk130_assertion type Assertion NP198789.RAMXn2U7O_lVcQzhAtkeu9rkO56H_U5opkRC3UDMDyrhk130_head.
- NP198789.RAMXn2U7O_lVcQzhAtkeu9rkO56H_U5opkRC3UDMDyrhk130_assertion description "[Almost 90% of the MODY cases in the group studied are explained by mutations in the major genes GCK (MODY2) and HNF-1alpha (MODY3), although differences in the relative prevalence of each form could be partly due to patient referral bias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP198789.RAMXn2U7O_lVcQzhAtkeu9rkO56H_U5opkRC3UDMDyrhk130_provenance.
- NP198789.RAMXn2U7O_lVcQzhAtkeu9rkO56H_U5opkRC3UDMDyrhk130_assertion evidence source_evidence_literature NP198789.RAMXn2U7O_lVcQzhAtkeu9rkO56H_U5opkRC3UDMDyrhk130_provenance.
- NP198789.RAMXn2U7O_lVcQzhAtkeu9rkO56H_U5opkRC3UDMDyrhk130_assertion SIO_000772 17573900 NP198789.RAMXn2U7O_lVcQzhAtkeu9rkO56H_U5opkRC3UDMDyrhk130_provenance.
- NP198789.RAMXn2U7O_lVcQzhAtkeu9rkO56H_U5opkRC3UDMDyrhk130_assertion wasDerivedFrom lhgdn-20090331 NP198789.RAMXn2U7O_lVcQzhAtkeu9rkO56H_U5opkRC3UDMDyrhk130_provenance.
- NP198789.RAMXn2U7O_lVcQzhAtkeu9rkO56H_U5opkRC3UDMDyrhk130_assertion wasGeneratedBy ECO_0000203 NP198789.RAMXn2U7O_lVcQzhAtkeu9rkO56H_U5opkRC3UDMDyrhk130_provenance.