Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP6204.RAy1AlOo2G3NlIAqgkmjD3AMGMiGmyTYEWIxVORygHN5o130_assertion> ?p ?o ?g. }
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- NP6204.RAy1AlOo2G3NlIAqgkmjD3AMGMiGmyTYEWIxVORygHN5o130_assertion type Assertion NP6204.RAy1AlOo2G3NlIAqgkmjD3AMGMiGmyTYEWIxVORygHN5o130_head.
- NP6204.RAy1AlOo2G3NlIAqgkmjD3AMGMiGmyTYEWIxVORygHN5o130_assertion description "[We then identified mutations in SLC6A19 in members of the original family in whom Hartnup disorder was discovered and of three Japanese families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6204.RAy1AlOo2G3NlIAqgkmjD3AMGMiGmyTYEWIxVORygHN5o130_provenance.
- NP6204.RAy1AlOo2G3NlIAqgkmjD3AMGMiGmyTYEWIxVORygHN5o130_assertion evidence source_evidence_curated NP6204.RAy1AlOo2G3NlIAqgkmjD3AMGMiGmyTYEWIxVORygHN5o130_provenance.
- NP6204.RAy1AlOo2G3NlIAqgkmjD3AMGMiGmyTYEWIxVORygHN5o130_assertion SIO_000772 15286787 NP6204.RAy1AlOo2G3NlIAqgkmjD3AMGMiGmyTYEWIxVORygHN5o130_provenance.
- NP6204.RAy1AlOo2G3NlIAqgkmjD3AMGMiGmyTYEWIxVORygHN5o130_assertion wasDerivedFrom uniprot-20130724 NP6204.RAy1AlOo2G3NlIAqgkmjD3AMGMiGmyTYEWIxVORygHN5o130_provenance.
- NP6204.RAy1AlOo2G3NlIAqgkmjD3AMGMiGmyTYEWIxVORygHN5o130_assertion wasGeneratedBy ECO_0000218 NP6204.RAy1AlOo2G3NlIAqgkmjD3AMGMiGmyTYEWIxVORygHN5o130_provenance.