Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP795190.RAQPWV_nEkxvPvubbJkKWpP42BKWSraF1yEmbOUYtAKoA130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP795190.RAQPWV_nEkxvPvubbJkKWpP42BKWSraF1yEmbOUYtAKoA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795190.RAQPWV_nEkxvPvubbJkKWpP42BKWSraF1yEmbOUYtAKoA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795190.RAQPWV_nEkxvPvubbJkKWpP42BKWSraF1yEmbOUYtAKoA130_provenance.
- NP795190.RAQPWV_nEkxvPvubbJkKWpP42BKWSraF1yEmbOUYtAKoA130_assertion description "[Comparisons of hypocretin deficiency and frequency of HLA-DQB1*0602-positivity in the Danish and eligible NC and NwC populations (included via MEDLINE search), by (re)calculation of study results using the ICSD-2 criterion for low CSF hcrt-1 (< 30% of normal mean).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP795190.RAQPWV_nEkxvPvubbJkKWpP42BKWSraF1yEmbOUYtAKoA130_provenance.
- NP795190.RAQPWV_nEkxvPvubbJkKWpP42BKWSraF1yEmbOUYtAKoA130_assertion evidence source_evidence_literature NP795190.RAQPWV_nEkxvPvubbJkKWpP42BKWSraF1yEmbOUYtAKoA130_provenance.
- NP795190.RAQPWV_nEkxvPvubbJkKWpP42BKWSraF1yEmbOUYtAKoA130_assertion SIO_000772 20175400 NP795190.RAQPWV_nEkxvPvubbJkKWpP42BKWSraF1yEmbOUYtAKoA130_provenance.
- NP795190.RAQPWV_nEkxvPvubbJkKWpP42BKWSraF1yEmbOUYtAKoA130_assertion wasDerivedFrom befree-2016 NP795190.RAQPWV_nEkxvPvubbJkKWpP42BKWSraF1yEmbOUYtAKoA130_provenance.
- NP795190.RAQPWV_nEkxvPvubbJkKWpP42BKWSraF1yEmbOUYtAKoA130_assertion wasGeneratedBy ECO_0000203 NP795190.RAQPWV_nEkxvPvubbJkKWpP42BKWSraF1yEmbOUYtAKoA130_provenance.
- befree-2016 importedOn "2016-02-19" NP795190.RAQPWV_nEkxvPvubbJkKWpP42BKWSraF1yEmbOUYtAKoA130_provenance.