Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP778575.RAFxhREx4AHVmpw53YBHAudPghILXtr9tOFhyhJlHQgAM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP778575.RAFxhREx4AHVmpw53YBHAudPghILXtr9tOFhyhJlHQgAM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP778575.RAFxhREx4AHVmpw53YBHAudPghILXtr9tOFhyhJlHQgAM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP778575.RAFxhREx4AHVmpw53YBHAudPghILXtr9tOFhyhJlHQgAM130_provenance.
- NP778575.RAFxhREx4AHVmpw53YBHAudPghILXtr9tOFhyhJlHQgAM130_assertion description "[A total of 1,389 Japanese patients with RA were genotyped for 30 single-nucleotide polymorphisms (SNPs) in the HLA region using commercial oligonucleotide arrays (from Perlegen or Affymetrix) as well as for HLA-DRB1 alleles using a sequence-specific polymerase chain reaction method.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP778575.RAFxhREx4AHVmpw53YBHAudPghILXtr9tOFhyhJlHQgAM130_provenance.
- NP778575.RAFxhREx4AHVmpw53YBHAudPghILXtr9tOFhyhJlHQgAM130_assertion evidence source_evidence_literature NP778575.RAFxhREx4AHVmpw53YBHAudPghILXtr9tOFhyhJlHQgAM130_provenance.
- NP778575.RAFxhREx4AHVmpw53YBHAudPghILXtr9tOFhyhJlHQgAM130_assertion SIO_000772 19950296 NP778575.RAFxhREx4AHVmpw53YBHAudPghILXtr9tOFhyhJlHQgAM130_provenance.
- NP778575.RAFxhREx4AHVmpw53YBHAudPghILXtr9tOFhyhJlHQgAM130_assertion wasDerivedFrom befree-2016 NP778575.RAFxhREx4AHVmpw53YBHAudPghILXtr9tOFhyhJlHQgAM130_provenance.
- NP778575.RAFxhREx4AHVmpw53YBHAudPghILXtr9tOFhyhJlHQgAM130_assertion wasGeneratedBy ECO_0000203 NP778575.RAFxhREx4AHVmpw53YBHAudPghILXtr9tOFhyhJlHQgAM130_provenance.
- befree-2016 importedOn "2016-02-19" NP778575.RAFxhREx4AHVmpw53YBHAudPghILXtr9tOFhyhJlHQgAM130_provenance.