Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP460684.RAZyKj0wCTwThKk8I8IoFKaQyj2Xu2YuLdpEg1rdlRMBc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP460684.RAZyKj0wCTwThKk8I8IoFKaQyj2Xu2YuLdpEg1rdlRMBc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP460684.RAZyKj0wCTwThKk8I8IoFKaQyj2Xu2YuLdpEg1rdlRMBc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP460684.RAZyKj0wCTwThKk8I8IoFKaQyj2Xu2YuLdpEg1rdlRMBc130_provenance.
- NP460684.RAZyKj0wCTwThKk8I8IoFKaQyj2Xu2YuLdpEg1rdlRMBc130_assertion description "[A Japanese case of congenital hyperinsulinism with hyperammonemia due to a mutation in glutamate dehydrogenase (GLUD1) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP460684.RAZyKj0wCTwThKk8I8IoFKaQyj2Xu2YuLdpEg1rdlRMBc130_provenance.
- NP460684.RAZyKj0wCTwThKk8I8IoFKaQyj2Xu2YuLdpEg1rdlRMBc130_assertion evidence source_evidence_literature NP460684.RAZyKj0wCTwThKk8I8IoFKaQyj2Xu2YuLdpEg1rdlRMBc130_provenance.
- NP460684.RAZyKj0wCTwThKk8I8IoFKaQyj2Xu2YuLdpEg1rdlRMBc130_assertion SIO_000772 11201367 NP460684.RAZyKj0wCTwThKk8I8IoFKaQyj2Xu2YuLdpEg1rdlRMBc130_provenance.
- NP460684.RAZyKj0wCTwThKk8I8IoFKaQyj2Xu2YuLdpEg1rdlRMBc130_assertion wasDerivedFrom befree-20140225 NP460684.RAZyKj0wCTwThKk8I8IoFKaQyj2Xu2YuLdpEg1rdlRMBc130_provenance.
- NP460684.RAZyKj0wCTwThKk8I8IoFKaQyj2Xu2YuLdpEg1rdlRMBc130_assertion wasGeneratedBy ECO_0000203 NP460684.RAZyKj0wCTwThKk8I8IoFKaQyj2Xu2YuLdpEg1rdlRMBc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP460684.RAZyKj0wCTwThKk8I8IoFKaQyj2Xu2YuLdpEg1rdlRMBc130_provenance.