Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP852722.RA4GdopJTtDSmn6DhR1H9mUr1QCzNZjPY1hn0Zum0Zm4c130_assertion> ?p ?o ?g. }
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- NP852722.RA4GdopJTtDSmn6DhR1H9mUr1QCzNZjPY1hn0Zum0Zm4c130_assertion type Assertion NP852722.RA4GdopJTtDSmn6DhR1H9mUr1QCzNZjPY1hn0Zum0Zm4c130_head.
- NP852722.RA4GdopJTtDSmn6DhR1H9mUr1QCzNZjPY1hn0Zum0Zm4c130_assertion description "[Subsequent studies demonstrated that this mutation is present in one-half of all CG1 patients and correlates with the Zellweger syndrome phenotype.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP852722.RA4GdopJTtDSmn6DhR1H9mUr1QCzNZjPY1hn0Zum0Zm4c130_provenance.
- NP852722.RA4GdopJTtDSmn6DhR1H9mUr1QCzNZjPY1hn0Zum0Zm4c130_assertion evidence source_evidence_literature NP852722.RA4GdopJTtDSmn6DhR1H9mUr1QCzNZjPY1hn0Zum0Zm4c130_provenance.
- NP852722.RA4GdopJTtDSmn6DhR1H9mUr1QCzNZjPY1hn0Zum0Zm4c130_assertion SIO_000772 10447258 NP852722.RA4GdopJTtDSmn6DhR1H9mUr1QCzNZjPY1hn0Zum0Zm4c130_provenance.
- NP852722.RA4GdopJTtDSmn6DhR1H9mUr1QCzNZjPY1hn0Zum0Zm4c130_assertion wasDerivedFrom befree-20140225 NP852722.RA4GdopJTtDSmn6DhR1H9mUr1QCzNZjPY1hn0Zum0Zm4c130_provenance.
- NP852722.RA4GdopJTtDSmn6DhR1H9mUr1QCzNZjPY1hn0Zum0Zm4c130_assertion wasGeneratedBy ECO_0000203 NP852722.RA4GdopJTtDSmn6DhR1H9mUr1QCzNZjPY1hn0Zum0Zm4c130_provenance.