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- source_evidence_literature type ECO_0000212 NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_provenance.
- NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_assertion description "[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." NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_provenance.
- NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_assertion evidence source_evidence_literature NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_provenance.
- NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_assertion SIO_000772 15277402 NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_provenance.
- NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_assertion wasDerivedFrom lhgdn-20090331 NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_provenance.
- NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_assertion wasGeneratedBy ECO_0000203 NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP206085.RAFqE04Jp_KgnJ2UgLY56cfMjauxVRr1BiEVuMN9yvtN0130_provenance.