Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP761161.RAstxrE6FE234S6Ac9aCufGGvSL3qpZYth3Jbo_BJpvfo130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP761161.RAstxrE6FE234S6Ac9aCufGGvSL3qpZYth3Jbo_BJpvfo130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP761161.RAstxrE6FE234S6Ac9aCufGGvSL3qpZYth3Jbo_BJpvfo130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP761161.RAstxrE6FE234S6Ac9aCufGGvSL3qpZYth3Jbo_BJpvfo130_provenance.
- NP761161.RAstxrE6FE234S6Ac9aCufGGvSL3qpZYth3Jbo_BJpvfo130_assertion description "[This study was conducted to report a family affected by benign hereditary chorea in which a large deletion including TTF1, PAX9, and other genes was identified and results in oligodontia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP761161.RAstxrE6FE234S6Ac9aCufGGvSL3qpZYth3Jbo_BJpvfo130_provenance.
- NP761161.RAstxrE6FE234S6Ac9aCufGGvSL3qpZYth3Jbo_BJpvfo130_assertion evidence source_evidence_literature NP761161.RAstxrE6FE234S6Ac9aCufGGvSL3qpZYth3Jbo_BJpvfo130_provenance.
- NP761161.RAstxrE6FE234S6Ac9aCufGGvSL3qpZYth3Jbo_BJpvfo130_assertion SIO_000772 18445003 NP761161.RAstxrE6FE234S6Ac9aCufGGvSL3qpZYth3Jbo_BJpvfo130_provenance.
- NP761161.RAstxrE6FE234S6Ac9aCufGGvSL3qpZYth3Jbo_BJpvfo130_assertion wasDerivedFrom befree-20150227 NP761161.RAstxrE6FE234S6Ac9aCufGGvSL3qpZYth3Jbo_BJpvfo130_provenance.
- NP761161.RAstxrE6FE234S6Ac9aCufGGvSL3qpZYth3Jbo_BJpvfo130_assertion wasGeneratedBy ECO_0000203 NP761161.RAstxrE6FE234S6Ac9aCufGGvSL3qpZYth3Jbo_BJpvfo130_provenance.
- befree-20150227 importedOn "2015-02-27" NP761161.RAstxrE6FE234S6Ac9aCufGGvSL3qpZYth3Jbo_BJpvfo130_provenance.