Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP542319.RArW-mbPHxdsEydmPPjSHTT7CgoXhCxKwfuia-sVc1WIM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP542319.RArW-mbPHxdsEydmPPjSHTT7CgoXhCxKwfuia-sVc1WIM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP542319.RArW-mbPHxdsEydmPPjSHTT7CgoXhCxKwfuia-sVc1WIM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP542319.RArW-mbPHxdsEydmPPjSHTT7CgoXhCxKwfuia-sVc1WIM130_provenance.
- NP542319.RArW-mbPHxdsEydmPPjSHTT7CgoXhCxKwfuia-sVc1WIM130_assertion description "[In blinded specimens and colon cancer cell lines with defined mutations, ColoSeq correctly identified 28/28 (100%) pathogenic mutations in MLH1, MSH2, MSH6, PMS2, EPCAM, APC, and MUTYH, including single nucleotide variants (SNVs), small insertions and deletions, and large copy number variants.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP542319.RArW-mbPHxdsEydmPPjSHTT7CgoXhCxKwfuia-sVc1WIM130_provenance.
- NP542319.RArW-mbPHxdsEydmPPjSHTT7CgoXhCxKwfuia-sVc1WIM130_assertion evidence source_evidence_literature NP542319.RArW-mbPHxdsEydmPPjSHTT7CgoXhCxKwfuia-sVc1WIM130_provenance.
- NP542319.RArW-mbPHxdsEydmPPjSHTT7CgoXhCxKwfuia-sVc1WIM130_assertion SIO_000772 22658618 NP542319.RArW-mbPHxdsEydmPPjSHTT7CgoXhCxKwfuia-sVc1WIM130_provenance.
- NP542319.RArW-mbPHxdsEydmPPjSHTT7CgoXhCxKwfuia-sVc1WIM130_assertion wasDerivedFrom befree-20150227 NP542319.RArW-mbPHxdsEydmPPjSHTT7CgoXhCxKwfuia-sVc1WIM130_provenance.
- NP542319.RArW-mbPHxdsEydmPPjSHTT7CgoXhCxKwfuia-sVc1WIM130_assertion wasGeneratedBy ECO_0000203 NP542319.RArW-mbPHxdsEydmPPjSHTT7CgoXhCxKwfuia-sVc1WIM130_provenance.
- befree-20150227 importedOn "2015-02-27" NP542319.RArW-mbPHxdsEydmPPjSHTT7CgoXhCxKwfuia-sVc1WIM130_provenance.