Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP2055.RARkhHbDy67GInS1EWdbUjJFUizYjwG-eGSYfJ1746RyY130_assertion> ?p ?o ?g. }
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- NP2055.RARkhHbDy67GInS1EWdbUjJFUizYjwG-eGSYfJ1746RyY130_assertion type Assertion NP2055.RARkhHbDy67GInS1EWdbUjJFUizYjwG-eGSYfJ1746RyY130_head.
- NP2055.RARkhHbDy67GInS1EWdbUjJFUizYjwG-eGSYfJ1746RyY130_assertion description "[In this article, we identify a gene, SLC39A4, located in the candidate region and, in patients with AE, document mutations that likely lead to the disease.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP2055.RARkhHbDy67GInS1EWdbUjJFUizYjwG-eGSYfJ1746RyY130_provenance.
- NP2055.RARkhHbDy67GInS1EWdbUjJFUizYjwG-eGSYfJ1746RyY130_assertion evidence source_evidence_curated NP2055.RARkhHbDy67GInS1EWdbUjJFUizYjwG-eGSYfJ1746RyY130_provenance.
- NP2055.RARkhHbDy67GInS1EWdbUjJFUizYjwG-eGSYfJ1746RyY130_assertion SIO_000772 12032886 NP2055.RARkhHbDy67GInS1EWdbUjJFUizYjwG-eGSYfJ1746RyY130_provenance.
- NP2055.RARkhHbDy67GInS1EWdbUjJFUizYjwG-eGSYfJ1746RyY130_assertion wasDerivedFrom uniprot-2016 NP2055.RARkhHbDy67GInS1EWdbUjJFUizYjwG-eGSYfJ1746RyY130_provenance.
- NP2055.RARkhHbDy67GInS1EWdbUjJFUizYjwG-eGSYfJ1746RyY130_assertion wasGeneratedBy ECO_0000218 NP2055.RARkhHbDy67GInS1EWdbUjJFUizYjwG-eGSYfJ1746RyY130_provenance.