Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_provenance.
- 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.
- befree-20140225 importedOn "2014-02-25" NP718068.RArd_Qt6mUeVtJaRTgWJ2CkJHn_PybWJNp3eikYrgl8GA130_provenance.