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- source_evidence_literature type ECO_0000212 NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_provenance.
- NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_assertion description "[Heterozygous inactivating mutations in the glucokinase gene (GCK) cause a mild form of diabetes (maturity-onset diabetes of the young [MODY]2), and activating mutations have been associated with a mild form of familial hyperinsulinemic hypoglycemia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_provenance.
- NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_assertion evidence source_evidence_literature NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_provenance.
- NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_assertion SIO_000772 15277402 NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_provenance.
- NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_assertion wasDerivedFrom befree-20150227 NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_provenance.
- NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_assertion wasGeneratedBy ECO_0000203 NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP420799.RAPq6CNKsWGIlm584BbI1vg9YMGVl8_bKQ11JBN8DTofI130_provenance.