Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP981917.RAT16T4Hbfvc7SXj6VfL3Hh5ENmcQY2CnzogO4wtw2rjs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP981917.RAT16T4Hbfvc7SXj6VfL3Hh5ENmcQY2CnzogO4wtw2rjs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP981917.RAT16T4Hbfvc7SXj6VfL3Hh5ENmcQY2CnzogO4wtw2rjs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP981917.RAT16T4Hbfvc7SXj6VfL3Hh5ENmcQY2CnzogO4wtw2rjs130_provenance.
- NP981917.RAT16T4Hbfvc7SXj6VfL3Hh5ENmcQY2CnzogO4wtw2rjs130_assertion description "[Among the human PEX genes associated with peroxisome biogenesis disorders, only the PEX11 family genes had not previously been associated with human disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP981917.RAT16T4Hbfvc7SXj6VfL3Hh5ENmcQY2CnzogO4wtw2rjs130_provenance.
- NP981917.RAT16T4Hbfvc7SXj6VfL3Hh5ENmcQY2CnzogO4wtw2rjs130_assertion evidence source_evidence_literature NP981917.RAT16T4Hbfvc7SXj6VfL3Hh5ENmcQY2CnzogO4wtw2rjs130_provenance.
- NP981917.RAT16T4Hbfvc7SXj6VfL3Hh5ENmcQY2CnzogO4wtw2rjs130_assertion SIO_000772 22581969 NP981917.RAT16T4Hbfvc7SXj6VfL3Hh5ENmcQY2CnzogO4wtw2rjs130_provenance.
- NP981917.RAT16T4Hbfvc7SXj6VfL3Hh5ENmcQY2CnzogO4wtw2rjs130_assertion wasDerivedFrom befree-2016 NP981917.RAT16T4Hbfvc7SXj6VfL3Hh5ENmcQY2CnzogO4wtw2rjs130_provenance.
- NP981917.RAT16T4Hbfvc7SXj6VfL3Hh5ENmcQY2CnzogO4wtw2rjs130_assertion wasGeneratedBy ECO_0000203 NP981917.RAT16T4Hbfvc7SXj6VfL3Hh5ENmcQY2CnzogO4wtw2rjs130_provenance.
- befree-2016 importedOn "2016-02-19" NP981917.RAT16T4Hbfvc7SXj6VfL3Hh5ENmcQY2CnzogO4wtw2rjs130_provenance.