Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP82650.RAtRQVH41vKqdd634rRBJVZYEEKlDGtavyJzy2AqEm0OQ130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP82650.RAtRQVH41vKqdd634rRBJVZYEEKlDGtavyJzy2AqEm0OQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP82650.RAtRQVH41vKqdd634rRBJVZYEEKlDGtavyJzy2AqEm0OQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP82650.RAtRQVH41vKqdd634rRBJVZYEEKlDGtavyJzy2AqEm0OQ130_provenance.
- NP82650.RAtRQVH41vKqdd634rRBJVZYEEKlDGtavyJzy2AqEm0OQ130_assertion description "[Genomic deletions in MSH2 or MLH1 are a frequent cause of hereditary non-polyposis colorectal cancer: identification of novel and recurrentdeletions by MLPA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP82650.RAtRQVH41vKqdd634rRBJVZYEEKlDGtavyJzy2AqEm0OQ130_provenance.
- NP82650.RAtRQVH41vKqdd634rRBJVZYEEKlDGtavyJzy2AqEm0OQ130_assertion evidence source_evidence_literature NP82650.RAtRQVH41vKqdd634rRBJVZYEEKlDGtavyJzy2AqEm0OQ130_provenance.
- NP82650.RAtRQVH41vKqdd634rRBJVZYEEKlDGtavyJzy2AqEm0OQ130_assertion SIO_000772 14635101 NP82650.RAtRQVH41vKqdd634rRBJVZYEEKlDGtavyJzy2AqEm0OQ130_provenance.
- NP82650.RAtRQVH41vKqdd634rRBJVZYEEKlDGtavyJzy2AqEm0OQ130_assertion wasDerivedFrom gad-20150221 NP82650.RAtRQVH41vKqdd634rRBJVZYEEKlDGtavyJzy2AqEm0OQ130_provenance.
- NP82650.RAtRQVH41vKqdd634rRBJVZYEEKlDGtavyJzy2AqEm0OQ130_assertion wasGeneratedBy ECO_0000203 NP82650.RAtRQVH41vKqdd634rRBJVZYEEKlDGtavyJzy2AqEm0OQ130_provenance.
- gad-20150221 importedOn "2015-02-21" NP82650.RAtRQVH41vKqdd634rRBJVZYEEKlDGtavyJzy2AqEm0OQ130_provenance.