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- source_evidence_literature type ECO_0000212 NP520898.RAHPggsTdTEoO-2xqkh4VH8DhYA_Su43sisEadNIJY0EA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP520898.RAHPggsTdTEoO-2xqkh4VH8DhYA_Su43sisEadNIJY0EA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP520898.RAHPggsTdTEoO-2xqkh4VH8DhYA_Su43sisEadNIJY0EA130_provenance.
- NP520898.RAHPggsTdTEoO-2xqkh4VH8DhYA_Su43sisEadNIJY0EA130_assertion description "[We confirmed that alleles of the 8.1 ancestral haplotype were important risk markers for the development of IIM, and a random forests classification analysis suggested that within this haplotype, HLA-B*0801, DRB1*0301 and/ or closely linked genes are the principal HLA risk factors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP520898.RAHPggsTdTEoO-2xqkh4VH8DhYA_Su43sisEadNIJY0EA130_provenance.
- NP520898.RAHPggsTdTEoO-2xqkh4VH8DhYA_Su43sisEadNIJY0EA130_assertion evidence source_evidence_literature NP520898.RAHPggsTdTEoO-2xqkh4VH8DhYA_Su43sisEadNIJY0EA130_provenance.
- NP520898.RAHPggsTdTEoO-2xqkh4VH8DhYA_Su43sisEadNIJY0EA130_assertion SIO_000772 16267409 NP520898.RAHPggsTdTEoO-2xqkh4VH8DhYA_Su43sisEadNIJY0EA130_provenance.
- NP520898.RAHPggsTdTEoO-2xqkh4VH8DhYA_Su43sisEadNIJY0EA130_assertion wasDerivedFrom befree-2016 NP520898.RAHPggsTdTEoO-2xqkh4VH8DhYA_Su43sisEadNIJY0EA130_provenance.
- NP520898.RAHPggsTdTEoO-2xqkh4VH8DhYA_Su43sisEadNIJY0EA130_assertion wasGeneratedBy ECO_0000203 NP520898.RAHPggsTdTEoO-2xqkh4VH8DhYA_Su43sisEadNIJY0EA130_provenance.
- befree-2016 importedOn "2016-02-19" NP520898.RAHPggsTdTEoO-2xqkh4VH8DhYA_Su43sisEadNIJY0EA130_provenance.