Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1009242.RAyFGIZ03kFNSqv4eWhGQ1qttFxQI07t5I1S8NHuxFTgs130_assertion> ?p ?o ?g. }
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- NP1009242.RAyFGIZ03kFNSqv4eWhGQ1qttFxQI07t5I1S8NHuxFTgs130_assertion type Assertion NP1009242.RAyFGIZ03kFNSqv4eWhGQ1qttFxQI07t5I1S8NHuxFTgs130_head.
- NP1009242.RAyFGIZ03kFNSqv4eWhGQ1qttFxQI07t5I1S8NHuxFTgs130_assertion description "[Urinary and plasma amines and amine metabolites were quantified in two individuals with Norrie disease resulting from a deletion in chromosomal region Xp11.3, recently reported to be associated with absence of the gene encoding monoamine oxidase (MAO)-A and nondetectable MAO-A activity in fibroblasts and MAO-B activity in platelets.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1009242.RAyFGIZ03kFNSqv4eWhGQ1qttFxQI07t5I1S8NHuxFTgs130_provenance.
- NP1009242.RAyFGIZ03kFNSqv4eWhGQ1qttFxQI07t5I1S8NHuxFTgs130_assertion evidence source_evidence_literature NP1009242.RAyFGIZ03kFNSqv4eWhGQ1qttFxQI07t5I1S8NHuxFTgs130_provenance.
- NP1009242.RAyFGIZ03kFNSqv4eWhGQ1qttFxQI07t5I1S8NHuxFTgs130_assertion SIO_000772 2293615 NP1009242.RAyFGIZ03kFNSqv4eWhGQ1qttFxQI07t5I1S8NHuxFTgs130_provenance.
- NP1009242.RAyFGIZ03kFNSqv4eWhGQ1qttFxQI07t5I1S8NHuxFTgs130_assertion wasDerivedFrom befree-2016 NP1009242.RAyFGIZ03kFNSqv4eWhGQ1qttFxQI07t5I1S8NHuxFTgs130_provenance.
- NP1009242.RAyFGIZ03kFNSqv4eWhGQ1qttFxQI07t5I1S8NHuxFTgs130_assertion wasGeneratedBy ECO_0000203 NP1009242.RAyFGIZ03kFNSqv4eWhGQ1qttFxQI07t5I1S8NHuxFTgs130_provenance.