This HTML5 document contains 35 embedded RDF statements represented using HTML+Microdata notation.
The embedded RDF content will be recognized by any processor of HTML5 Microdata.
| Prefix | Namespace IRI |
|---|---|
| framestercore | https://w3id.org/framester/data/framestercore/ |
| n7 | https://w3id.org/framester/data/framestersyn/Fanconi_s_anemia.n. |
| n32 | https://w3id.org/framester/data/framestersyn/Ichthyosis.n. |
| n24 | https://w3id.org/framester/data/framestersyn/Hepatolenticular_degeneration.n. |
| n19 | https://w3id.org/framester/data/framestersyn/Oligodontia.n. |
| n16 | https://w3id.org/framester/data/framestersyn/Autosomal_dominant_disease.n. |
| n21 | https://w3id.org/framester/data/framestersyn/Nevoid_elephantiasis.n. |
| n33 | https://w3id.org/framester/data/framestersyn/Abetalipoproteinemia.n. |
| n23 | https://w3id.org/framester/data/framestersyn/McArdle_s_disease.n. |
| n34 | https://w3id.org/framester/data/framestersyn/Achondroplasia.n. |
| rdfs | http://www.w3.org/2000/01/rdf-schema# |
| n28 | https://w3id.org/framester/data/framestersyn/Porphyria.n. |
| n31 | https://w3id.org/framester/data/framestersyn/Spielmeyer-Vogt_disease.n. |
| n6 | https://w3id.org/framester/data/framestersyn/Congenital_afibrinogenemia.n. |
| n25 | https://w3id.org/framester/data/framestersyn/Autosomal_recessive_disease.n. |
| n11 | https://w3id.org/framester/data/framestersyn/Otosclerosis.n. |
| n26 | https://w3id.org/framester/data/framestersyn/Dwarfism.n. |
| n2 | https://w3id.org/framester/data/framestersyn/Lactose_intolerance.n. |
| n12 | https://w3id.org/framester/data/framestersyn/Oligodactyly.n. |
| n14 | https://w3id.org/framester/data/framestersyn/Muscular_dystrophy.n. |
| n27 | https://w3id.org/framester/data/framestersyn/Monogenic_disorder.n. |
| rdf | http://www.w3.org/1999/02/22-rdf-syntax-ns# |
| n30 | https://w3id.org/framester/data/framestersyn/Maple_syrup_urine_disease.n. |
| wn30instances | https://w3id.org/framester/wn/wn30/instances/ |
| owl | http://www.w3.org/2002/07/owl# |
| n17 | https://w3id.org/framester/data/framestersyn/Osteopetrosis.n. |
| n9 | https://w3id.org/framester/data/framestersyn/Polygenic_disorder.n. |
| n8 | https://w3id.org/framester/data/framestersyn/Hyperbetalipoproteinemia.n. |
| n13 | https://w3id.org/framester/data/framestersyn/Inborn_error_of_metabolism.n. |
| xsdh | http://www.w3.org/2001/XMLSchema# |
| n22 | https://w3id.org/framester/data/framestersyn/Mucopolysaccharidosis.n. |
| n4 | https://w3id.org/framester/data/framestersyn/Genetic_disease.n. |
| fschema | https://w3id.org/framester/schema/ |
| n29 | https://w3id.org/framester/data/framestersyn/Hirschsprung_s_disease.n. |
| n5 | https://w3id.org/framester/data/framestersyn/Disease.n. |