Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_assertion> ?p ?o ?g. }
Showing items 1 to 6 of
6
with 100 items per page.
- NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_assertion type Assertion NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_head.
- NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_assertion description "[These findings demonstrate that the range of the clinical phenotype caused by GCK mutations varies from complete insulin deficiency to extreme hyperinsulinemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_provenance.
- NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_assertion evidence source_evidence_literature NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_provenance.
- NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_assertion SIO_000772 15277402 NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_provenance.
- NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_assertion wasDerivedFrom befree-20140225 NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_provenance.
- NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_assertion wasGeneratedBy ECO_0000203 NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_provenance.