Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP795188.RA6p768bMrTpn1hcNim42C8i-t703dzW7zHikP0O6rWsY130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP795188.RA6p768bMrTpn1hcNim42C8i-t703dzW7zHikP0O6rWsY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP795188.RA6p768bMrTpn1hcNim42C8i-t703dzW7zHikP0O6rWsY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP795188.RA6p768bMrTpn1hcNim42C8i-t703dzW7zHikP0O6rWsY130_provenance.
- NP795188.RA6p768bMrTpn1hcNim42C8i-t703dzW7zHikP0O6rWsY130_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." NP795188.RA6p768bMrTpn1hcNim42C8i-t703dzW7zHikP0O6rWsY130_provenance.
- NP795188.RA6p768bMrTpn1hcNim42C8i-t703dzW7zHikP0O6rWsY130_assertion evidence source_evidence_literature NP795188.RA6p768bMrTpn1hcNim42C8i-t703dzW7zHikP0O6rWsY130_provenance.
- NP795188.RA6p768bMrTpn1hcNim42C8i-t703dzW7zHikP0O6rWsY130_assertion SIO_000772 20175400 NP795188.RA6p768bMrTpn1hcNim42C8i-t703dzW7zHikP0O6rWsY130_provenance.
- NP795188.RA6p768bMrTpn1hcNim42C8i-t703dzW7zHikP0O6rWsY130_assertion wasDerivedFrom befree-2016 NP795188.RA6p768bMrTpn1hcNim42C8i-t703dzW7zHikP0O6rWsY130_provenance.
- NP795188.RA6p768bMrTpn1hcNim42C8i-t703dzW7zHikP0O6rWsY130_assertion wasGeneratedBy ECO_0000203 NP795188.RA6p768bMrTpn1hcNim42C8i-t703dzW7zHikP0O6rWsY130_provenance.
- befree-2016 importedOn "2016-02-19" NP795188.RA6p768bMrTpn1hcNim42C8i-t703dzW7zHikP0O6rWsY130_provenance.