Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP588083.RARoLxK7i296qAhUmgKwVgIaYzr2y75jHyF08vEjtAji4130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP588083.RARoLxK7i296qAhUmgKwVgIaYzr2y75jHyF08vEjtAji4130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP588083.RARoLxK7i296qAhUmgKwVgIaYzr2y75jHyF08vEjtAji4130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP588083.RARoLxK7i296qAhUmgKwVgIaYzr2y75jHyF08vEjtAji4130_provenance.
- NP588083.RARoLxK7i296qAhUmgKwVgIaYzr2y75jHyF08vEjtAji4130_assertion description "[The CHEK2 1100delC was not significantly increased in Swedish colorectal cancer patients, however, in order to determine the role of the variant in colorectal cancer families with the history of breast cancer a larger sample size is needed.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP588083.RARoLxK7i296qAhUmgKwVgIaYzr2y75jHyF08vEjtAji4130_provenance.
- NP588083.RARoLxK7i296qAhUmgKwVgIaYzr2y75jHyF08vEjtAji4130_assertion evidence source_evidence_literature NP588083.RARoLxK7i296qAhUmgKwVgIaYzr2y75jHyF08vEjtAji4130_provenance.
- NP588083.RARoLxK7i296qAhUmgKwVgIaYzr2y75jHyF08vEjtAji4130_assertion SIO_000772 17214356 NP588083.RARoLxK7i296qAhUmgKwVgIaYzr2y75jHyF08vEjtAji4130_provenance.
- NP588083.RARoLxK7i296qAhUmgKwVgIaYzr2y75jHyF08vEjtAji4130_assertion wasDerivedFrom befree-2016 NP588083.RARoLxK7i296qAhUmgKwVgIaYzr2y75jHyF08vEjtAji4130_provenance.
- NP588083.RARoLxK7i296qAhUmgKwVgIaYzr2y75jHyF08vEjtAji4130_assertion wasGeneratedBy ECO_0000203 NP588083.RARoLxK7i296qAhUmgKwVgIaYzr2y75jHyF08vEjtAji4130_provenance.
- befree-2016 importedOn "2016-02-19" NP588083.RARoLxK7i296qAhUmgKwVgIaYzr2y75jHyF08vEjtAji4130_provenance.