Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_provenance.
- NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_assertion description "[Manitoba aboriginal kindred with original cerebro-oculo- facio-skeletal syndrome has a mutation in the Cockayne syndrome group B (CSB) gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_provenance.
- NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_assertion evidence source_evidence_literature NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_provenance.
- NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_assertion SIO_000772 10739753 NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_provenance.
- NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_assertion wasDerivedFrom befree-20140225 NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_provenance.
- NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_assertion wasGeneratedBy ECO_0000203 NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_provenance.
- befree-20140225 importedOn "2014-02-25" NP694218.RAsMApJB8TWPUXUUs1bybhVJg7FsxhmQqBFJU4P2PHtgc130_provenance.