Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1005284.RAzaR14l2-Mvlp6S3B6HFNCD76GCvomiTiXIsuhWLJzpk130_assertion> ?p ?o ?g. }
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- NP1005284.RAzaR14l2-Mvlp6S3B6HFNCD76GCvomiTiXIsuhWLJzpk130_assertion type Assertion NP1005284.RAzaR14l2-Mvlp6S3B6HFNCD76GCvomiTiXIsuhWLJzpk130_head.
- NP1005284.RAzaR14l2-Mvlp6S3B6HFNCD76GCvomiTiXIsuhWLJzpk130_assertion wasGeneratedBy ECO_0000203 NP1005284.RAzaR14l2-Mvlp6S3B6HFNCD76GCvomiTiXIsuhWLJzpk130_provenance.
- NP1005284.RAzaR14l2-Mvlp6S3B6HFNCD76GCvomiTiXIsuhWLJzpk130_assertion wasDerivedFrom befree-2016 NP1005284.RAzaR14l2-Mvlp6S3B6HFNCD76GCvomiTiXIsuhWLJzpk130_provenance.
- NP1005284.RAzaR14l2-Mvlp6S3B6HFNCD76GCvomiTiXIsuhWLJzpk130_assertion SIO_000772 22894767 NP1005284.RAzaR14l2-Mvlp6S3B6HFNCD76GCvomiTiXIsuhWLJzpk130_provenance.
- NP1005284.RAzaR14l2-Mvlp6S3B6HFNCD76GCvomiTiXIsuhWLJzpk130_assertion evidence source_evidence_literature NP1005284.RAzaR14l2-Mvlp6S3B6HFNCD76GCvomiTiXIsuhWLJzpk130_provenance.
- NP1005284.RAzaR14l2-Mvlp6S3B6HFNCD76GCvomiTiXIsuhWLJzpk130_assertion description "[A founder mutation in the PEX6 gene is responsible for increased incidence of Zellweger syndrome in a French Canadian population.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1005284.RAzaR14l2-Mvlp6S3B6HFNCD76GCvomiTiXIsuhWLJzpk130_provenance.