Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP335867.RAFygE8tMdokb-ryGQW77IUoU352M76s0tlmF-T1fjO0o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP335867.RAFygE8tMdokb-ryGQW77IUoU352M76s0tlmF-T1fjO0o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP335867.RAFygE8tMdokb-ryGQW77IUoU352M76s0tlmF-T1fjO0o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP335867.RAFygE8tMdokb-ryGQW77IUoU352M76s0tlmF-T1fjO0o130_provenance.
- NP335867.RAFygE8tMdokb-ryGQW77IUoU352M76s0tlmF-T1fjO0o130_assertion description "[We investigated two single-nucleotide polymorphisms (SNPs) in PDCD1 and five polymorphisms in CTLA4 in 102 patients with AAV and 188 healthy controls (HC).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP335867.RAFygE8tMdokb-ryGQW77IUoU352M76s0tlmF-T1fjO0o130_provenance.
- NP335867.RAFygE8tMdokb-ryGQW77IUoU352M76s0tlmF-T1fjO0o130_assertion evidence source_evidence_literature NP335867.RAFygE8tMdokb-ryGQW77IUoU352M76s0tlmF-T1fjO0o130_provenance.
- NP335867.RAFygE8tMdokb-ryGQW77IUoU352M76s0tlmF-T1fjO0o130_assertion SIO_000772 18448390 NP335867.RAFygE8tMdokb-ryGQW77IUoU352M76s0tlmF-T1fjO0o130_provenance.
- NP335867.RAFygE8tMdokb-ryGQW77IUoU352M76s0tlmF-T1fjO0o130_assertion wasDerivedFrom befree-20150227 NP335867.RAFygE8tMdokb-ryGQW77IUoU352M76s0tlmF-T1fjO0o130_provenance.
- NP335867.RAFygE8tMdokb-ryGQW77IUoU352M76s0tlmF-T1fjO0o130_assertion wasGeneratedBy ECO_0000203 NP335867.RAFygE8tMdokb-ryGQW77IUoU352M76s0tlmF-T1fjO0o130_provenance.
- befree-20150227 importedOn "2015-02-27" NP335867.RAFygE8tMdokb-ryGQW77IUoU352M76s0tlmF-T1fjO0o130_provenance.