Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP454073.RAbKt9qFYvRz5_QuCyWXm99gV3sKh-OKfDrEk0i5KbQRI130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP454073.RAbKt9qFYvRz5_QuCyWXm99gV3sKh-OKfDrEk0i5KbQRI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP454073.RAbKt9qFYvRz5_QuCyWXm99gV3sKh-OKfDrEk0i5KbQRI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP454073.RAbKt9qFYvRz5_QuCyWXm99gV3sKh-OKfDrEk0i5KbQRI130_provenance.
- NP454073.RAbKt9qFYvRz5_QuCyWXm99gV3sKh-OKfDrEk0i5KbQRI130_assertion description "[Patients were included either when hypocretin deficiency was documented (CSF hypocretin-1?110 pg/ml, n=91) or on the basis of the presence of clear cataplexy and HLA-DQB1?0602 positivity (n=419).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP454073.RAbKt9qFYvRz5_QuCyWXm99gV3sKh-OKfDrEk0i5KbQRI130_provenance.
- NP454073.RAbKt9qFYvRz5_QuCyWXm99gV3sKh-OKfDrEk0i5KbQRI130_assertion evidence source_evidence_literature NP454073.RAbKt9qFYvRz5_QuCyWXm99gV3sKh-OKfDrEk0i5KbQRI130_provenance.
- NP454073.RAbKt9qFYvRz5_QuCyWXm99gV3sKh-OKfDrEk0i5KbQRI130_assertion SIO_000772 22177342 NP454073.RAbKt9qFYvRz5_QuCyWXm99gV3sKh-OKfDrEk0i5KbQRI130_provenance.
- NP454073.RAbKt9qFYvRz5_QuCyWXm99gV3sKh-OKfDrEk0i5KbQRI130_assertion wasDerivedFrom befree-20150227 NP454073.RAbKt9qFYvRz5_QuCyWXm99gV3sKh-OKfDrEk0i5KbQRI130_provenance.
- NP454073.RAbKt9qFYvRz5_QuCyWXm99gV3sKh-OKfDrEk0i5KbQRI130_assertion wasGeneratedBy ECO_0000203 NP454073.RAbKt9qFYvRz5_QuCyWXm99gV3sKh-OKfDrEk0i5KbQRI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP454073.RAbKt9qFYvRz5_QuCyWXm99gV3sKh-OKfDrEk0i5KbQRI130_provenance.