Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP117119.RAd8W4lot4GWQ0XlRUZ2HygXh2nEVYLqSHxZ79_-bmSXw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP117119.RAd8W4lot4GWQ0XlRUZ2HygXh2nEVYLqSHxZ79_-bmSXw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP117119.RAd8W4lot4GWQ0XlRUZ2HygXh2nEVYLqSHxZ79_-bmSXw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP117119.RAd8W4lot4GWQ0XlRUZ2HygXh2nEVYLqSHxZ79_-bmSXw130_provenance.
- NP117119.RAd8W4lot4GWQ0XlRUZ2HygXh2nEVYLqSHxZ79_-bmSXw130_assertion description "[We typed Norwegian MS patients (n = 631) and controls (n = 555) for HLA-A, -B, -C and -DRB1 alleles as well as the presence or absence of genes encoding inhibitory (KIR2DL1, KIR2DL2, KIR2DL3, KIR2DL5, KIR3DL1, KIR3DL2, KIR3DL3) and activating (KIR2DS1, KIR2DS2, KIR2DS3, KIR2DL4, KIR2DS4, KIR2DS5, KIR3DS1) KIRs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP117119.RAd8W4lot4GWQ0XlRUZ2HygXh2nEVYLqSHxZ79_-bmSXw130_provenance.
- NP117119.RAd8W4lot4GWQ0XlRUZ2HygXh2nEVYLqSHxZ79_-bmSXw130_assertion evidence source_evidence_literature NP117119.RAd8W4lot4GWQ0XlRUZ2HygXh2nEVYLqSHxZ79_-bmSXw130_provenance.
- NP117119.RAd8W4lot4GWQ0XlRUZ2HygXh2nEVYLqSHxZ79_-bmSXw130_assertion SIO_000772 19630074 NP117119.RAd8W4lot4GWQ0XlRUZ2HygXh2nEVYLqSHxZ79_-bmSXw130_provenance.
- NP117119.RAd8W4lot4GWQ0XlRUZ2HygXh2nEVYLqSHxZ79_-bmSXw130_assertion wasDerivedFrom gad-20150221 NP117119.RAd8W4lot4GWQ0XlRUZ2HygXh2nEVYLqSHxZ79_-bmSXw130_provenance.
- NP117119.RAd8W4lot4GWQ0XlRUZ2HygXh2nEVYLqSHxZ79_-bmSXw130_assertion wasGeneratedBy ECO_0000203 NP117119.RAd8W4lot4GWQ0XlRUZ2HygXh2nEVYLqSHxZ79_-bmSXw130_provenance.
- gad-20150221 importedOn "2015-02-21" NP117119.RAd8W4lot4GWQ0XlRUZ2HygXh2nEVYLqSHxZ79_-bmSXw130_provenance.