Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP135579.RAGODnNbu2NdXCuhe8Z8xm3mbnmKzFXyaag1Mqtz5bfr0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP135579.RAGODnNbu2NdXCuhe8Z8xm3mbnmKzFXyaag1Mqtz5bfr0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP135579.RAGODnNbu2NdXCuhe8Z8xm3mbnmKzFXyaag1Mqtz5bfr0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP135579.RAGODnNbu2NdXCuhe8Z8xm3mbnmKzFXyaag1Mqtz5bfr0130_provenance.
- NP135579.RAGODnNbu2NdXCuhe8Z8xm3mbnmKzFXyaag1Mqtz5bfr0130_assertion description "[Almost 90% of the MODY cases in the group studied are explained by mutations in the major genes GCK (MODY2) and HNF-1alpha (MODY3), although differences in the relative prevalence of each form could be partly due to patient referral bias.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP135579.RAGODnNbu2NdXCuhe8Z8xm3mbnmKzFXyaag1Mqtz5bfr0130_provenance.
- NP135579.RAGODnNbu2NdXCuhe8Z8xm3mbnmKzFXyaag1Mqtz5bfr0130_assertion evidence source_evidence_literature NP135579.RAGODnNbu2NdXCuhe8Z8xm3mbnmKzFXyaag1Mqtz5bfr0130_provenance.
- NP135579.RAGODnNbu2NdXCuhe8Z8xm3mbnmKzFXyaag1Mqtz5bfr0130_assertion SIO_000772 17573900 NP135579.RAGODnNbu2NdXCuhe8Z8xm3mbnmKzFXyaag1Mqtz5bfr0130_provenance.
- NP135579.RAGODnNbu2NdXCuhe8Z8xm3mbnmKzFXyaag1Mqtz5bfr0130_assertion wasDerivedFrom lhgdn-20090331 NP135579.RAGODnNbu2NdXCuhe8Z8xm3mbnmKzFXyaag1Mqtz5bfr0130_provenance.
- NP135579.RAGODnNbu2NdXCuhe8Z8xm3mbnmKzFXyaag1Mqtz5bfr0130_assertion wasGeneratedBy ECO_0000203 NP135579.RAGODnNbu2NdXCuhe8Z8xm3mbnmKzFXyaag1Mqtz5bfr0130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP135579.RAGODnNbu2NdXCuhe8Z8xm3mbnmKzFXyaag1Mqtz5bfr0130_provenance.