Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP224192.RAlP-6M26AeDos6EGLODf9QlIZV0nZOwtZQl-lvVCvgzQ130_assertion> ?p ?o ?g. }
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- NP224192.RAlP-6M26AeDos6EGLODf9QlIZV0nZOwtZQl-lvVCvgzQ130_assertion type Assertion NP224192.RAlP-6M26AeDos6EGLODf9QlIZV0nZOwtZQl-lvVCvgzQ130_head.
- NP224192.RAlP-6M26AeDos6EGLODf9QlIZV0nZOwtZQl-lvVCvgzQ130_assertion description "[Spectrum of mutations and sequence variants in the FALDH gene in patients with Sj�gren-Larsson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP224192.RAlP-6M26AeDos6EGLODf9QlIZV0nZOwtZQl-lvVCvgzQ130_provenance.
- NP224192.RAlP-6M26AeDos6EGLODf9QlIZV0nZOwtZQl-lvVCvgzQ130_assertion evidence source_evidence_literature NP224192.RAlP-6M26AeDos6EGLODf9QlIZV0nZOwtZQl-lvVCvgzQ130_provenance.
- NP224192.RAlP-6M26AeDos6EGLODf9QlIZV0nZOwtZQl-lvVCvgzQ130_assertion SIO_000772 9829906 NP224192.RAlP-6M26AeDos6EGLODf9QlIZV0nZOwtZQl-lvVCvgzQ130_provenance.
- NP224192.RAlP-6M26AeDos6EGLODf9QlIZV0nZOwtZQl-lvVCvgzQ130_assertion wasDerivedFrom befree-20150227 NP224192.RAlP-6M26AeDos6EGLODf9QlIZV0nZOwtZQl-lvVCvgzQ130_provenance.
- NP224192.RAlP-6M26AeDos6EGLODf9QlIZV0nZOwtZQl-lvVCvgzQ130_assertion wasGeneratedBy ECO_0000203 NP224192.RAlP-6M26AeDos6EGLODf9QlIZV0nZOwtZQl-lvVCvgzQ130_provenance.