Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP528103.RAhhEzJzO-bqBhAh2GKqyYFMFNLQhGFP6aCa-2W4x8DHc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP528103.RAhhEzJzO-bqBhAh2GKqyYFMFNLQhGFP6aCa-2W4x8DHc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP528103.RAhhEzJzO-bqBhAh2GKqyYFMFNLQhGFP6aCa-2W4x8DHc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP528103.RAhhEzJzO-bqBhAh2GKqyYFMFNLQhGFP6aCa-2W4x8DHc130_provenance.
- befree-20150227 importedOn "2015-02-27" NP528103.RAhhEzJzO-bqBhAh2GKqyYFMFNLQhGFP6aCa-2W4x8DHc130_provenance.
- NP528103.RAhhEzJzO-bqBhAh2GKqyYFMFNLQhGFP6aCa-2W4x8DHc130_assertion wasGeneratedBy ECO_0000203 NP528103.RAhhEzJzO-bqBhAh2GKqyYFMFNLQhGFP6aCa-2W4x8DHc130_provenance.
- NP528103.RAhhEzJzO-bqBhAh2GKqyYFMFNLQhGFP6aCa-2W4x8DHc130_assertion wasDerivedFrom befree-20150227 NP528103.RAhhEzJzO-bqBhAh2GKqyYFMFNLQhGFP6aCa-2W4x8DHc130_provenance.
- NP528103.RAhhEzJzO-bqBhAh2GKqyYFMFNLQhGFP6aCa-2W4x8DHc130_assertion SIO_000772 17204026 NP528103.RAhhEzJzO-bqBhAh2GKqyYFMFNLQhGFP6aCa-2W4x8DHc130_provenance.
- NP528103.RAhhEzJzO-bqBhAh2GKqyYFMFNLQhGFP6aCa-2W4x8DHc130_assertion evidence source_evidence_literature NP528103.RAhhEzJzO-bqBhAh2GKqyYFMFNLQhGFP6aCa-2W4x8DHc130_provenance.
- NP528103.RAhhEzJzO-bqBhAh2GKqyYFMFNLQhGFP6aCa-2W4x8DHc130_assertion description "[In this review the morphological correlates of five molecular subtypes are outlined: Type 1 (CIMP-high/MSI-H/BRAF mutation), Type 2 (CIMP-high/MSI-L or MSS/BRAF mutation), Type 3 (CIMP-low/MSS or MSI-L/KRAS mutation), Type 4 (CIMP-neg/MSS) and Type 5 or Lynch syndrome (CIMP-neg/MSI-H).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP528103.RAhhEzJzO-bqBhAh2GKqyYFMFNLQhGFP6aCa-2W4x8DHc130_provenance.