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- source_evidence_literature type ECO_0000212 NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_provenance.
- NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_assertion description "[Molecular analysis of 250 patients with autosomal recessive congenital ichthyosis: evidence for mutation hotspots in ALOXE3 and allelic heterogeneity in ALOX12B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_provenance.
- NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_assertion evidence source_evidence_literature NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_provenance.
- NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_assertion SIO_000772 19131948 NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_provenance.
- NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_assertion wasDerivedFrom gad-20130706 NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_provenance.
- NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_assertion wasGeneratedBy ECO_0000203 NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_provenance.
- gad-20130706 importedOn "2013-07-06" NP79500.RAy8D2pIr8N4FcjK6ZYizMq0OM0FPbVJvmfZYw1zEhpvY130_provenance.