Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP718356.RAmNdwTufQvZQxs2BKLX1njmOh33prmlh2W_OZERa9th0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP718356.RAmNdwTufQvZQxs2BKLX1njmOh33prmlh2W_OZERa9th0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP718356.RAmNdwTufQvZQxs2BKLX1njmOh33prmlh2W_OZERa9th0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP718356.RAmNdwTufQvZQxs2BKLX1njmOh33prmlh2W_OZERa9th0130_provenance.
- NP718356.RAmNdwTufQvZQxs2BKLX1njmOh33prmlh2W_OZERa9th0130_assertion description "[About three quarters of the HLA DQB1*0602 positive patients with narcolepsy and cataplexy had low CSF hypocretin-1 values, and appear to form a distinct clinical entity.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP718356.RAmNdwTufQvZQxs2BKLX1njmOh33prmlh2W_OZERa9th0130_provenance.
- NP718356.RAmNdwTufQvZQxs2BKLX1njmOh33prmlh2W_OZERa9th0130_assertion evidence source_evidence_literature NP718356.RAmNdwTufQvZQxs2BKLX1njmOh33prmlh2W_OZERa9th0130_provenance.
- NP718356.RAmNdwTufQvZQxs2BKLX1njmOh33prmlh2W_OZERa9th0130_assertion SIO_000772 17702265 NP718356.RAmNdwTufQvZQxs2BKLX1njmOh33prmlh2W_OZERa9th0130_provenance.
- NP718356.RAmNdwTufQvZQxs2BKLX1njmOh33prmlh2W_OZERa9th0130_assertion wasDerivedFrom befree-20140225 NP718356.RAmNdwTufQvZQxs2BKLX1njmOh33prmlh2W_OZERa9th0130_provenance.
- NP718356.RAmNdwTufQvZQxs2BKLX1njmOh33prmlh2W_OZERa9th0130_assertion wasGeneratedBy ECO_0000203 NP718356.RAmNdwTufQvZQxs2BKLX1njmOh33prmlh2W_OZERa9th0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP718356.RAmNdwTufQvZQxs2BKLX1njmOh33prmlh2W_OZERa9th0130_provenance.