Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP868023.RACKi2WN0xPgY_rK5GLhHbrWAw4wDNnu8tEVa0bgrkwMs130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP868023.RACKi2WN0xPgY_rK5GLhHbrWAw4wDNnu8tEVa0bgrkwMs130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP868023.RACKi2WN0xPgY_rK5GLhHbrWAw4wDNnu8tEVa0bgrkwMs130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP868023.RACKi2WN0xPgY_rK5GLhHbrWAw4wDNnu8tEVa0bgrkwMs130_provenance.
- NP868023.RACKi2WN0xPgY_rK5GLhHbrWAw4wDNnu8tEVa0bgrkwMs130_assertion description "[Genetic defects in human pericentrin (PCNT), encoding the centrosomal protein pericentrin, cause a form of osteodysplastic primordial dwarfism that is sometimes reported to be associated with diabetes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP868023.RACKi2WN0xPgY_rK5GLhHbrWAw4wDNnu8tEVa0bgrkwMs130_provenance.
- NP868023.RACKi2WN0xPgY_rK5GLhHbrWAw4wDNnu8tEVa0bgrkwMs130_assertion evidence source_evidence_literature NP868023.RACKi2WN0xPgY_rK5GLhHbrWAw4wDNnu8tEVa0bgrkwMs130_provenance.
- NP868023.RACKi2WN0xPgY_rK5GLhHbrWAw4wDNnu8tEVa0bgrkwMs130_assertion SIO_000772 21270239 NP868023.RACKi2WN0xPgY_rK5GLhHbrWAw4wDNnu8tEVa0bgrkwMs130_provenance.
- NP868023.RACKi2WN0xPgY_rK5GLhHbrWAw4wDNnu8tEVa0bgrkwMs130_assertion wasDerivedFrom befree-2016 NP868023.RACKi2WN0xPgY_rK5GLhHbrWAw4wDNnu8tEVa0bgrkwMs130_provenance.
- NP868023.RACKi2WN0xPgY_rK5GLhHbrWAw4wDNnu8tEVa0bgrkwMs130_assertion wasGeneratedBy ECO_0000203 NP868023.RACKi2WN0xPgY_rK5GLhHbrWAw4wDNnu8tEVa0bgrkwMs130_provenance.
- befree-2016 importedOn "2016-02-19" NP868023.RACKi2WN0xPgY_rK5GLhHbrWAw4wDNnu8tEVa0bgrkwMs130_provenance.