Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_assertion> ?p ?o ?g. }
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- NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_assertion type Assertion NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_head.
- NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_assertion wasGeneratedBy ECO_0000203 NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_provenance.
- NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_assertion wasDerivedFrom befree-20140225 NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_provenance.
- NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_assertion SIO_000772 20844025 NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_provenance.
- NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_assertion evidence source_evidence_literature NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_provenance.
- NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_assertion description "[We studied an adult patient with ORD due to homozygous POR A287P, the most frequent POR mutation in Caucasians, and her clinically unaffected, heterozygous mother.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP455984.RAie5NVIBtNdoZ5KmNjefTYf2MykI1IFHMdCukNYwpKT8130_provenance.