Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP502187.RAXhvTEZs7LCDmHJfPHga8f9lauPGXWu4NSAD37AXRLvM130_assertion> ?p ?o ?g. }
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- NP502187.RAXhvTEZs7LCDmHJfPHga8f9lauPGXWu4NSAD37AXRLvM130_assertion type Assertion NP502187.RAXhvTEZs7LCDmHJfPHga8f9lauPGXWu4NSAD37AXRLvM130_head.
- NP502187.RAXhvTEZs7LCDmHJfPHga8f9lauPGXWu4NSAD37AXRLvM130_assertion description "[These results demonstrate that mutation in PEX16 is the genetic cause of CG-D PBDs.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP502187.RAXhvTEZs7LCDmHJfPHga8f9lauPGXWu4NSAD37AXRLvM130_provenance.
- NP502187.RAXhvTEZs7LCDmHJfPHga8f9lauPGXWu4NSAD37AXRLvM130_assertion evidence source_evidence_literature NP502187.RAXhvTEZs7LCDmHJfPHga8f9lauPGXWu4NSAD37AXRLvM130_provenance.
- NP502187.RAXhvTEZs7LCDmHJfPHga8f9lauPGXWu4NSAD37AXRLvM130_assertion SIO_000772 9837814 NP502187.RAXhvTEZs7LCDmHJfPHga8f9lauPGXWu4NSAD37AXRLvM130_provenance.
- NP502187.RAXhvTEZs7LCDmHJfPHga8f9lauPGXWu4NSAD37AXRLvM130_assertion wasDerivedFrom befree-20140225 NP502187.RAXhvTEZs7LCDmHJfPHga8f9lauPGXWu4NSAD37AXRLvM130_provenance.
- NP502187.RAXhvTEZs7LCDmHJfPHga8f9lauPGXWu4NSAD37AXRLvM130_assertion wasGeneratedBy ECO_0000203 NP502187.RAXhvTEZs7LCDmHJfPHga8f9lauPGXWu4NSAD37AXRLvM130_provenance.