Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1135301.RA4Xn0qVmIRZOi1isFsvM4mPVAMDhmiyqR8qt0gFAeukA130_assertion> ?p ?o ?g. }
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- NP1135301.RA4Xn0qVmIRZOi1isFsvM4mPVAMDhmiyqR8qt0gFAeukA130_assertion type Assertion NP1135301.RA4Xn0qVmIRZOi1isFsvM4mPVAMDhmiyqR8qt0gFAeukA130_head.
- NP1135301.RA4Xn0qVmIRZOi1isFsvM4mPVAMDhmiyqR8qt0gFAeukA130_assertion description "[In our cohort of MODY patients from two national centres the de novo mutations in GCK, HNF1A and HNF4A were present in 7.3% of the 150 families without a history of diabetes and 1.2% of all of the referrals for MODY testing.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1135301.RA4Xn0qVmIRZOi1isFsvM4mPVAMDhmiyqR8qt0gFAeukA130_provenance.
- NP1135301.RA4Xn0qVmIRZOi1isFsvM4mPVAMDhmiyqR8qt0gFAeukA130_assertion evidence source_evidence_literature NP1135301.RA4Xn0qVmIRZOi1isFsvM4mPVAMDhmiyqR8qt0gFAeukA130_provenance.
- NP1135301.RA4Xn0qVmIRZOi1isFsvM4mPVAMDhmiyqR8qt0gFAeukA130_assertion SIO_000772 24323243 NP1135301.RA4Xn0qVmIRZOi1isFsvM4mPVAMDhmiyqR8qt0gFAeukA130_provenance.
- NP1135301.RA4Xn0qVmIRZOi1isFsvM4mPVAMDhmiyqR8qt0gFAeukA130_assertion wasDerivedFrom befree-2016 NP1135301.RA4Xn0qVmIRZOi1isFsvM4mPVAMDhmiyqR8qt0gFAeukA130_provenance.
- NP1135301.RA4Xn0qVmIRZOi1isFsvM4mPVAMDhmiyqR8qt0gFAeukA130_assertion wasGeneratedBy ECO_0000203 NP1135301.RA4Xn0qVmIRZOi1isFsvM4mPVAMDhmiyqR8qt0gFAeukA130_provenance.