http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo#head http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo#assertion http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo#provenance http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo#assertion http://rdf.disgenet.org/resource/gda/DGN0eafe1d9554e6fefbcd2697aa6014657 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/4920 http://rdf.disgenet.org/resource/gda/DGN0eafe1d9554e6fefbcd2697aa6014657 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0265205 http://rdf.disgenet.org/resource/gda/DGN0eafe1d9554e6fefbcd2697aa6014657 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo#provenance http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo#assertion http://purl.org/dc/terms/description [The same gene, ROR2, has been shown to cause autosomal dominant brachydactyly B, but it is not known at present whether the autosomal dominant form of Robinow syndrome is also caused by mutations in ROR2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo#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/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/12011143 http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo#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/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo http://purl.org/dc/terms/created 2017-10-17T13:15:06+02:00 http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP772077.RANbe_uW-NtOf94DTnwpeKtgBpbpaOK3duJq6v_MtEtpo 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