Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP133316.RAwFmVJQPQN6N-FpjucjT8sdkd6tK-HuSmnVVljBSAMhM130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP133316.RAwFmVJQPQN6N-FpjucjT8sdkd6tK-HuSmnVVljBSAMhM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP133316.RAwFmVJQPQN6N-FpjucjT8sdkd6tK-HuSmnVVljBSAMhM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP133316.RAwFmVJQPQN6N-FpjucjT8sdkd6tK-HuSmnVVljBSAMhM130_provenance.
- NP133316.RAwFmVJQPQN6N-FpjucjT8sdkd6tK-HuSmnVVljBSAMhM130_assertion description "[We investigated whether putatively functional single nucleotide polymorphisms (SNPs) in genes related to CIN (CENPF, ESPL1, NEK2, PTTG1, ZWILCH, ZWINT) affect breast cancer (BC) risk and clinical outcome in a Swedish cohort of 749 incident BC cases with detailed clinical data and up to 15 years of follow-up and 1493 matched controls.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP133316.RAwFmVJQPQN6N-FpjucjT8sdkd6tK-HuSmnVVljBSAMhM130_provenance.
- NP133316.RAwFmVJQPQN6N-FpjucjT8sdkd6tK-HuSmnVVljBSAMhM130_assertion evidence source_evidence_literature NP133316.RAwFmVJQPQN6N-FpjucjT8sdkd6tK-HuSmnVVljBSAMhM130_provenance.
- NP133316.RAwFmVJQPQN6N-FpjucjT8sdkd6tK-HuSmnVVljBSAMhM130_assertion SIO_000772 19008095 NP133316.RAwFmVJQPQN6N-FpjucjT8sdkd6tK-HuSmnVVljBSAMhM130_provenance.
- NP133316.RAwFmVJQPQN6N-FpjucjT8sdkd6tK-HuSmnVVljBSAMhM130_assertion wasDerivedFrom gad-20150221 NP133316.RAwFmVJQPQN6N-FpjucjT8sdkd6tK-HuSmnVVljBSAMhM130_provenance.
- NP133316.RAwFmVJQPQN6N-FpjucjT8sdkd6tK-HuSmnVVljBSAMhM130_assertion wasGeneratedBy ECO_0000203 NP133316.RAwFmVJQPQN6N-FpjucjT8sdkd6tK-HuSmnVVljBSAMhM130_provenance.
- gad-20150221 importedOn "2015-02-21" NP133316.RAwFmVJQPQN6N-FpjucjT8sdkd6tK-HuSmnVVljBSAMhM130_provenance.