Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance.
- NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_assertion description "[We sought somatic mutations in the corresponding genes in the CRCs of the patients harboring the germline lesions and found biallelic inactivation of FANCM, LAMB4, PTCHD3, LAMC3, and TREX2, potentially implicating these genes as tumor suppressors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance.
- NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_assertion evidence source_evidence_literature NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance.
- NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_assertion SIO_000772 23585368 NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance.
- NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_assertion wasDerivedFrom befree-20140225 NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance.
- NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_assertion wasGeneratedBy ECO_0000203 NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance.
- befree-20140225 importedOn "2014-02-25" NP894153.RAZ2YAIZhYzeHH2f0sZ5cber4YrahLbPLwKhTn8CEQvhg130_provenance.