Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130_provenance.
- NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130_assertion description "[our data suggested that CYP1B1 germ line-inactivating mutations might increase the incidence of HCA in women with HNF1alpha mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130_provenance.
- NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130_assertion evidence source_evidence_literature NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130_provenance.
- NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130_assertion SIO_000772 17363580 NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130_provenance.
- NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130_assertion wasDerivedFrom gad-20130706 NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130_provenance.
- NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130_assertion wasGeneratedBy ECO_0000203 NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130_provenance.
- gad-20130706 importedOn "2013-07-06" NP66085.RAVMScAl6Vk1Cps7svJoCDqqtwfhtMSJFNwDVUK6FMMMY130_provenance.