Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP795196.RAbEyGxl4gHy7SJrFhCI9r3v4PiSzYI4RhU0vgKyvCOA4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP795196.RAbEyGxl4gHy7SJrFhCI9r3v4PiSzYI4RhU0vgKyvCOA4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795196.RAbEyGxl4gHy7SJrFhCI9r3v4PiSzYI4RhU0vgKyvCOA4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795196.RAbEyGxl4gHy7SJrFhCI9r3v4PiSzYI4RhU0vgKyvCOA4130_provenance.
- NP795196.RAbEyGxl4gHy7SJrFhCI9r3v4PiSzYI4RhU0vgKyvCOA4130_assertion description "[Across populations, low CSF hcrt-1 and HLA-DQB1*0602-positivity characterized the majority of NC (80% to 100%, P = 0.53; 80% to 100%, P = 0.11) but a minority of NwC patients (11% to 29%, P = 0.75; 29% to 89%, P = 0.043).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795196.RAbEyGxl4gHy7SJrFhCI9r3v4PiSzYI4RhU0vgKyvCOA4130_provenance.
- NP795196.RAbEyGxl4gHy7SJrFhCI9r3v4PiSzYI4RhU0vgKyvCOA4130_assertion evidence source_evidence_literature NP795196.RAbEyGxl4gHy7SJrFhCI9r3v4PiSzYI4RhU0vgKyvCOA4130_provenance.
- NP795196.RAbEyGxl4gHy7SJrFhCI9r3v4PiSzYI4RhU0vgKyvCOA4130_assertion SIO_000772 20175400 NP795196.RAbEyGxl4gHy7SJrFhCI9r3v4PiSzYI4RhU0vgKyvCOA4130_provenance.
- NP795196.RAbEyGxl4gHy7SJrFhCI9r3v4PiSzYI4RhU0vgKyvCOA4130_assertion wasDerivedFrom befree-2016 NP795196.RAbEyGxl4gHy7SJrFhCI9r3v4PiSzYI4RhU0vgKyvCOA4130_provenance.
- NP795196.RAbEyGxl4gHy7SJrFhCI9r3v4PiSzYI4RhU0vgKyvCOA4130_assertion wasGeneratedBy ECO_0000203 NP795196.RAbEyGxl4gHy7SJrFhCI9r3v4PiSzYI4RhU0vgKyvCOA4130_provenance.
- befree-2016 importedOn "2016-02-19" NP795196.RAbEyGxl4gHy7SJrFhCI9r3v4PiSzYI4RhU0vgKyvCOA4130_provenance.