Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1034848.RAWPZZbL8sHPOfweZWYdpa8BP_W6I6fxD4QpIUg6onJks130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP1034848.RAWPZZbL8sHPOfweZWYdpa8BP_W6I6fxD4QpIUg6onJks130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1034848.RAWPZZbL8sHPOfweZWYdpa8BP_W6I6fxD4QpIUg6onJks130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1034848.RAWPZZbL8sHPOfweZWYdpa8BP_W6I6fxD4QpIUg6onJks130_provenance.
- NP1034848.RAWPZZbL8sHPOfweZWYdpa8BP_W6I6fxD4QpIUg6onJks130_assertion description "[Unlike microsatellite unstable CRCs where hypermethylation of the DNA mismatch repair (MMR) gene hMLH1's promoter is causal, the precise cause of EMAST is not clearly defined but points towards hMSH3 deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1034848.RAWPZZbL8sHPOfweZWYdpa8BP_W6I6fxD4QpIUg6onJks130_provenance.
- NP1034848.RAWPZZbL8sHPOfweZWYdpa8BP_W6I6fxD4QpIUg6onJks130_assertion evidence source_evidence_literature NP1034848.RAWPZZbL8sHPOfweZWYdpa8BP_W6I6fxD4QpIUg6onJks130_provenance.
- NP1034848.RAWPZZbL8sHPOfweZWYdpa8BP_W6I6fxD4QpIUg6onJks130_assertion SIO_000772 23226332 NP1034848.RAWPZZbL8sHPOfweZWYdpa8BP_W6I6fxD4QpIUg6onJks130_provenance.
- NP1034848.RAWPZZbL8sHPOfweZWYdpa8BP_W6I6fxD4QpIUg6onJks130_assertion wasDerivedFrom befree-2016 NP1034848.RAWPZZbL8sHPOfweZWYdpa8BP_W6I6fxD4QpIUg6onJks130_provenance.
- NP1034848.RAWPZZbL8sHPOfweZWYdpa8BP_W6I6fxD4QpIUg6onJks130_assertion wasGeneratedBy ECO_0000203 NP1034848.RAWPZZbL8sHPOfweZWYdpa8BP_W6I6fxD4QpIUg6onJks130_provenance.
- befree-2016 importedOn "2016-02-19" NP1034848.RAWPZZbL8sHPOfweZWYdpa8BP_W6I6fxD4QpIUg6onJks130_provenance.