Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP370127.RAS4xL_dyzyizHsBb97cNoez20M9ylEnzJe9j1I73YQd4130_assertion> ?p ?o ?g. }
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- NP370127.RAS4xL_dyzyizHsBb97cNoez20M9ylEnzJe9j1I73YQd4130_assertion type Assertion NP370127.RAS4xL_dyzyizHsBb97cNoez20M9ylEnzJe9j1I73YQd4130_head.
- NP370127.RAS4xL_dyzyizHsBb97cNoez20M9ylEnzJe9j1I73YQd4130_assertion wasGeneratedBy ECO_0000203 NP370127.RAS4xL_dyzyizHsBb97cNoez20M9ylEnzJe9j1I73YQd4130_provenance.
- NP370127.RAS4xL_dyzyizHsBb97cNoez20M9ylEnzJe9j1I73YQd4130_assertion wasDerivedFrom befree-20140225 NP370127.RAS4xL_dyzyizHsBb97cNoez20M9ylEnzJe9j1I73YQd4130_provenance.
- NP370127.RAS4xL_dyzyizHsBb97cNoez20M9ylEnzJe9j1I73YQd4130_assertion SIO_000772 20844025 NP370127.RAS4xL_dyzyizHsBb97cNoez20M9ylEnzJe9j1I73YQd4130_provenance.
- NP370127.RAS4xL_dyzyizHsBb97cNoez20M9ylEnzJe9j1I73YQd4130_assertion evidence source_evidence_literature NP370127.RAS4xL_dyzyizHsBb97cNoez20M9ylEnzJe9j1I73YQd4130_provenance.
- NP370127.RAS4xL_dyzyizHsBb97cNoez20M9ylEnzJe9j1I73YQd4130_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." NP370127.RAS4xL_dyzyizHsBb97cNoez20M9ylEnzJe9j1I73YQd4130_provenance.