Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP331261.RAn75t2xupvO_LcNmGg-FpLhP5HF5V0bWN3bpWUzyAv1o130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP331261.RAn75t2xupvO_LcNmGg-FpLhP5HF5V0bWN3bpWUzyAv1o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP331261.RAn75t2xupvO_LcNmGg-FpLhP5HF5V0bWN3bpWUzyAv1o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP331261.RAn75t2xupvO_LcNmGg-FpLhP5HF5V0bWN3bpWUzyAv1o130_provenance.
- NP331261.RAn75t2xupvO_LcNmGg-FpLhP5HF5V0bWN3bpWUzyAv1o130_assertion description "[Three hundred seventy subjects, including 111 healthy controls, 93 narcoleptic subjects with hypocretin deficiency (cerebrospinal fluid [CSF] hypocretin-1 levels < 110 pg/mL), 72 narcoleptic subjects with normal hypocretin levels, and 89 subjects with other sleep disorders]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP331261.RAn75t2xupvO_LcNmGg-FpLhP5HF5V0bWN3bpWUzyAv1o130_provenance.
- NP331261.RAn75t2xupvO_LcNmGg-FpLhP5HF5V0bWN3bpWUzyAv1o130_assertion evidence source_evidence_literature NP331261.RAn75t2xupvO_LcNmGg-FpLhP5HF5V0bWN3bpWUzyAv1o130_provenance.
- NP331261.RAn75t2xupvO_LcNmGg-FpLhP5HF5V0bWN3bpWUzyAv1o130_assertion SIO_000772 16944669 NP331261.RAn75t2xupvO_LcNmGg-FpLhP5HF5V0bWN3bpWUzyAv1o130_provenance.
- NP331261.RAn75t2xupvO_LcNmGg-FpLhP5HF5V0bWN3bpWUzyAv1o130_assertion wasDerivedFrom befree-20150227 NP331261.RAn75t2xupvO_LcNmGg-FpLhP5HF5V0bWN3bpWUzyAv1o130_provenance.
- NP331261.RAn75t2xupvO_LcNmGg-FpLhP5HF5V0bWN3bpWUzyAv1o130_assertion wasGeneratedBy ECO_0000203 NP331261.RAn75t2xupvO_LcNmGg-FpLhP5HF5V0bWN3bpWUzyAv1o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP331261.RAn75t2xupvO_LcNmGg-FpLhP5HF5V0bWN3bpWUzyAv1o130_provenance.