http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0#head http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0#assertion http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0#provenance http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0#assertion http://rdf.disgenet.org/resource/gda/DGN864f6090207de57ed3864efc1030e62a http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/100038246 http://rdf.disgenet.org/resource/gda/DGN864f6090207de57ed3864efc1030e62a http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0039743 http://rdf.disgenet.org/resource/gda/DGN864f6090207de57ed3864efc1030e62a http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0#provenance http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0#assertion http://purl.org/dc/terms/description [The achondroplasia class of chondrodysplasias comprises the most common genetic forms of dwarfism in humans and includes achondroplasia, hypochondroplasia and thanatophoric dysplasia types I and II (TDI and TDII), which are caused by different mutations in a fibroblast growth-factor receptor FGFR3 (ref.1).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/9069288 http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://purl.org/dc/terms/created 2017-10-17T13:19:27+02:00 http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1459147.RA9j4G9ynH3a_9C1LW-3HdNLMc-ThyO6Jm8ENk6St0ze0 http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0