Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP169173.RAdX50Fh81imrdx7036tZcrMtSclO5gbUifmJzRUvEuQQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP169173.RAdX50Fh81imrdx7036tZcrMtSclO5gbUifmJzRUvEuQQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP169173.RAdX50Fh81imrdx7036tZcrMtSclO5gbUifmJzRUvEuQQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP169173.RAdX50Fh81imrdx7036tZcrMtSclO5gbUifmJzRUvEuQQ130_provenance.
- NP169173.RAdX50Fh81imrdx7036tZcrMtSclO5gbUifmJzRUvEuQQ130_assertion description "[We sequenced the MLH1/MSH2 coding and promoter core regions in patients with cancers suggestive of hereditary non-polyposis colorectal cancer, and correlated deleterious mutations with clinical and tumour features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP169173.RAdX50Fh81imrdx7036tZcrMtSclO5gbUifmJzRUvEuQQ130_provenance.
- NP169173.RAdX50Fh81imrdx7036tZcrMtSclO5gbUifmJzRUvEuQQ130_assertion evidence source_evidence_literature NP169173.RAdX50Fh81imrdx7036tZcrMtSclO5gbUifmJzRUvEuQQ130_provenance.
- NP169173.RAdX50Fh81imrdx7036tZcrMtSclO5gbUifmJzRUvEuQQ130_assertion SIO_000772 15996210 NP169173.RAdX50Fh81imrdx7036tZcrMtSclO5gbUifmJzRUvEuQQ130_provenance.
- NP169173.RAdX50Fh81imrdx7036tZcrMtSclO5gbUifmJzRUvEuQQ130_assertion wasDerivedFrom lhgdn-20090331 NP169173.RAdX50Fh81imrdx7036tZcrMtSclO5gbUifmJzRUvEuQQ130_provenance.
- NP169173.RAdX50Fh81imrdx7036tZcrMtSclO5gbUifmJzRUvEuQQ130_assertion wasGeneratedBy ECO_0000203 NP169173.RAdX50Fh81imrdx7036tZcrMtSclO5gbUifmJzRUvEuQQ130_provenance.
- lhgdn-20090331 importedOn "2009-03-31" NP169173.RAdX50Fh81imrdx7036tZcrMtSclO5gbUifmJzRUvEuQQ130_provenance.