Chromosome 20 - CaLiGraph

Property	Value
rdf:type	Chromosome (human) owl:NamedIndividual Disease MeSH code (G14) Gene on human chromosome 20 Congenital disorder MeSH code (A11)
rdfs:label	Chromosome 20
owl:sameAs	dbr:Chromosome_20
prov:wasDerivedFrom	http://en.wikipedia.org/wiki/Category:Chromosomes_(human) http://en.wikipedia.org/wiki/Lists_of_human_genes http://en.wikipedia.org/wiki/List_of_diseases_(C) http://en.wikipedia.org/wiki/List_of_MeSH_codes_(G14) http://en.wikipedia.org/wiki/Category:Genes_on_human_chromosome_20 http://en.wikipedia.org/wiki/List_of_MeSH_codes_(A11) http://en.wikipedia.org/wiki/Vertebrate_Genome_Annotation_Project http://en.wikipedia.org/wiki/List_of_congenital_disorders
skos:prefLabel	Chromosome 20
skos:altLabel	20 20p13 20q13.32 20th chromosome Chromosome 19, trisomy 19q Chromosome 22, trisomy chromosome 20 chromosome 20q11.2 chromosome 20q12-q13 chromosomes, human, pair 19 chromosomes, human, pair 21

About: clgr:Chromosome_20