Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP682889.RArRlEHLyYj3mecvnvZyEvcklWYwN_xQrxhtth7tVV_PY130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP682889.RArRlEHLyYj3mecvnvZyEvcklWYwN_xQrxhtth7tVV_PY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP682889.RArRlEHLyYj3mecvnvZyEvcklWYwN_xQrxhtth7tVV_PY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP682889.RArRlEHLyYj3mecvnvZyEvcklWYwN_xQrxhtth7tVV_PY130_provenance.
- NP682889.RArRlEHLyYj3mecvnvZyEvcklWYwN_xQrxhtth7tVV_PY130_assertion description "[After haplotype reconstruction, logistic regression analyses adjusted for traditional risk factors and COPD showed a significant association among AAA and AHCY, FOLH1, MTHFD1, MTR, NNMT, PON1 and TYMS haplotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP682889.RArRlEHLyYj3mecvnvZyEvcklWYwN_xQrxhtth7tVV_PY130_provenance.
- NP682889.RArRlEHLyYj3mecvnvZyEvcklWYwN_xQrxhtth7tVV_PY130_assertion evidence source_evidence_literature NP682889.RArRlEHLyYj3mecvnvZyEvcklWYwN_xQrxhtth7tVV_PY130_provenance.
- NP682889.RArRlEHLyYj3mecvnvZyEvcklWYwN_xQrxhtth7tVV_PY130_assertion SIO_000772 18635682 NP682889.RArRlEHLyYj3mecvnvZyEvcklWYwN_xQrxhtth7tVV_PY130_provenance.
- NP682889.RArRlEHLyYj3mecvnvZyEvcklWYwN_xQrxhtth7tVV_PY130_assertion wasDerivedFrom befree-2016 NP682889.RArRlEHLyYj3mecvnvZyEvcklWYwN_xQrxhtth7tVV_PY130_provenance.
- NP682889.RArRlEHLyYj3mecvnvZyEvcklWYwN_xQrxhtth7tVV_PY130_assertion wasGeneratedBy ECO_0000203 NP682889.RArRlEHLyYj3mecvnvZyEvcklWYwN_xQrxhtth7tVV_PY130_provenance.
- befree-2016 importedOn "2016-02-19" NP682889.RArRlEHLyYj3mecvnvZyEvcklWYwN_xQrxhtth7tVV_PY130_provenance.