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- source_evidence_literature type ECO_0000212 NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_provenance.
- NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_assertion description "[Defective DDX11 is associated with a unique cellular phenotype in which features of Fanconi anemia (drug-induced chromosomal breakage) and Roberts syndrome (sister chromatid cohesion defects) coexist.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_provenance.
- NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_assertion evidence source_evidence_literature NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_provenance.
- NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_assertion SIO_000772 20137776 NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_provenance.
- NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_assertion wasDerivedFrom befree-20140225 NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_provenance.
- NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_assertion wasGeneratedBy ECO_0000203 NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_provenance.
- befree-20140225 importedOn "2014-02-25" NP541748.RANuoP68-Zdw9AqYRKwKoTJReansLXoMT_jWS6m1XoooE130_provenance.