{"prefix":"genatlas","name":"Genatlas","description":"GenAtlas is a database containing information on human genes, markers and phenotypes.","pattern":"^\\w+$","uri_format":"http://genatlas.medecine.univ-paris5.fr/fiche.php?symbol=$1","providers":[{"code":"bio2rdf","name":"Bio2RDF","description":"Bio2RDF is an open-source project that uses Semantic Web technologies to build and provide the largest network of Linked Data for the Life Sciences. Bio2RDF defines a set of simple conventions to create RDF(S) compatible Linked Data from a diverse set of heterogeneously formatted sources obtained from multiple data providers.","homepage":"https://bio2rdf.org","uri_format":"http://bio2rdf.org/genatlas:$1"}],"homepage":"http://genatlas.medecine.univ-paris5.fr/","example":"HBB","example_extras":[],"deprecated":false,"mappings":{"biocontext":"GENATLAS","integbio":"nbdc00275","miriam":"genatlas","n2t":"genatlas","prefixcommons":"genatlas","uniprot":"DB-0027"},"synonyms":[],"keywords":["bibliography/documents","disorder","expression","gene","genome/gene","health/disease","human","organism-specific databases","phenotype","protein","rna","sequence"],"publications":[{"pubmed":"9835018","doi":"10.1016/s0764-4469(99)80021-3","title":"Genatlas database, genes and development defects","year":1998},{"pubmed":"10444337","doi":"10.1006/mgme.1999.2867","title":"Human genes involved in chromatin remodeling in transcription initiation, and associated diseases: An overview using the GENATLAS database","year":1999}],"appears_in":[],"depends_on":[],"namespace_in_lui":false,"preferred_prefix":"genatlas"}