Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP234339.RA9vXMqgJeKmALYsz6k2rNW1DlwitSTScM_GZda0gC4BM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP234339.RA9vXMqgJeKmALYsz6k2rNW1DlwitSTScM_GZda0gC4BM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP234339.RA9vXMqgJeKmALYsz6k2rNW1DlwitSTScM_GZda0gC4BM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP234339.RA9vXMqgJeKmALYsz6k2rNW1DlwitSTScM_GZda0gC4BM130_provenance.
- NP234339.RA9vXMqgJeKmALYsz6k2rNW1DlwitSTScM_GZda0gC4BM130_assertion description "[Haplotype D was associated with a nonstatistically significant increased risk of ovarian cancer overall and a statistically significant increased risk of invasive clear cell ovarian cancer.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP234339.RA9vXMqgJeKmALYsz6k2rNW1DlwitSTScM_GZda0gC4BM130_provenance.
- NP234339.RA9vXMqgJeKmALYsz6k2rNW1DlwitSTScM_GZda0gC4BM130_assertion evidence source_evidence_literature NP234339.RA9vXMqgJeKmALYsz6k2rNW1DlwitSTScM_GZda0gC4BM130_provenance.
- NP234339.RA9vXMqgJeKmALYsz6k2rNW1DlwitSTScM_GZda0gC4BM130_assertion SIO_000772 18268123 NP234339.RA9vXMqgJeKmALYsz6k2rNW1DlwitSTScM_GZda0gC4BM130_provenance.
- NP234339.RA9vXMqgJeKmALYsz6k2rNW1DlwitSTScM_GZda0gC4BM130_assertion wasDerivedFrom lhgdn-20090331 NP234339.RA9vXMqgJeKmALYsz6k2rNW1DlwitSTScM_GZda0gC4BM130_provenance.
- NP234339.RA9vXMqgJeKmALYsz6k2rNW1DlwitSTScM_GZda0gC4BM130_assertion wasGeneratedBy ECO_0000203 NP234339.RA9vXMqgJeKmALYsz6k2rNW1DlwitSTScM_GZda0gC4BM130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP234339.RA9vXMqgJeKmALYsz6k2rNW1DlwitSTScM_GZda0gC4BM130_provenance.