Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP270690.RA6_qCZmINLVQrJ0o92HsfXliP1Nmm3M-ViFACTJ6gUB8130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP270690.RA6_qCZmINLVQrJ0o92HsfXliP1Nmm3M-ViFACTJ6gUB8130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP270690.RA6_qCZmINLVQrJ0o92HsfXliP1Nmm3M-ViFACTJ6gUB8130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP270690.RA6_qCZmINLVQrJ0o92HsfXliP1Nmm3M-ViFACTJ6gUB8130_provenance.
- NP270690.RA6_qCZmINLVQrJ0o92HsfXliP1Nmm3M-ViFACTJ6gUB8130_assertion description "[Our data indicate that a common variant of the CD18 gene confers increased risk for CSS and MP, supporting that genetic factors are involved in the etiology and pathogenesis of ANCA-associated systemic vasculitides.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP270690.RA6_qCZmINLVQrJ0o92HsfXliP1Nmm3M-ViFACTJ6gUB8130_provenance.
- NP270690.RA6_qCZmINLVQrJ0o92HsfXliP1Nmm3M-ViFACTJ6gUB8130_assertion evidence source_evidence_literature NP270690.RA6_qCZmINLVQrJ0o92HsfXliP1Nmm3M-ViFACTJ6gUB8130_provenance.
- NP270690.RA6_qCZmINLVQrJ0o92HsfXliP1Nmm3M-ViFACTJ6gUB8130_assertion SIO_000772 10607485 NP270690.RA6_qCZmINLVQrJ0o92HsfXliP1Nmm3M-ViFACTJ6gUB8130_provenance.
- NP270690.RA6_qCZmINLVQrJ0o92HsfXliP1Nmm3M-ViFACTJ6gUB8130_assertion wasDerivedFrom befree-2016 NP270690.RA6_qCZmINLVQrJ0o92HsfXliP1Nmm3M-ViFACTJ6gUB8130_provenance.
- NP270690.RA6_qCZmINLVQrJ0o92HsfXliP1Nmm3M-ViFACTJ6gUB8130_assertion wasGeneratedBy ECO_0000203 NP270690.RA6_qCZmINLVQrJ0o92HsfXliP1Nmm3M-ViFACTJ6gUB8130_provenance.
- befree-2016 importedOn "2016-02-19" NP270690.RA6_qCZmINLVQrJ0o92HsfXliP1Nmm3M-ViFACTJ6gUB8130_provenance.