Statements in which the resource exists as a subject.
PredicateObject
rdf:type
relontology:expressedInOrga...
relontology:encodeProtein
entrezgene:hasGeneId
14359
entrezgene:unigeneReference
entrezgene:pubmed
pubmed-article:10349636, pubmed-article:10409431, pubmed-article:10922068, pubmed-article:11042159, pubmed-article:11076861, pubmed-article:11178106, pubmed-article:11217851, pubmed-article:11438699, pubmed-article:11544199, pubmed-article:11735223, pubmed-article:12466851, pubmed-article:12477932, pubmed-article:12520002, pubmed-article:12904583, pubmed-article:14610273, pubmed-article:15128702, pubmed-article:15489334, pubmed-article:15548538, pubmed-article:15782199, pubmed-article:16000371, pubmed-article:16033648, pubmed-article:16141072, pubmed-article:16141073, pubmed-article:16602821, pubmed-article:16930510, pubmed-article:17170008, pubmed-article:17868361, pubmed-article:17967808, pubmed-article:18589395, pubmed-article:18790697, pubmed-article:18799693, pubmed-article:19075228, pubmed-article:19487368, pubmed-article:20491901, pubmed-article:20530197, pubmed-article:20975687, pubmed-article:21589869, pubmed-article:21659647, pubmed-article:21677750, pubmed-article:21957233, pubmed-article:22022532, pubmed-article:8634689, pubmed-article:8889548
entrezgene:otherDesignation
fragile X mental retardation gene, autosomal homolog, fragile X mental retardation syndrome-related protein 1, fragile X mental retardation-related protein 1, fragile-X-related protein 1, mFxr1p
entrezgene:nucleotideAccess...
entrezgene:expressedIn
entrezgene:mapLocation
3|3 B
entrezgene:genomicAccession
entrezgene:stsReference
entrezgene:proteinAccession
entrezgene:uniprotAccession
entrezgene:dbXref
entrezgene:genomeAnnotation
entrezgene:chromosome
3
entrezgene:synonym
1110050J02Rik, 9530073J07Rik, AI851072, Fxr1h, Fxr1p
entrezgene:relationship
entrezgene:interaction
entrezgene:geneType
protein-coding
entrezgene:ensemblReference
entrezgene:goTerm
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