http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k#head
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k#assertion
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k#provenance
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k#assertion
http://rdf.disgenet.org/resource/gda/DGNab3c43048a90da7fd74018481d6f9599
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/2332
http://rdf.disgenet.org/resource/gda/DGNab3c43048a90da7fd74018481d6f9599
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0234376
http://rdf.disgenet.org/resource/gda/DGNab3c43048a90da7fd74018481d6f9599
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k#provenance
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k#assertion
http://purl.org/dc/terms/description
[Since male premutation carriers are relatively common in the general population, older men with ataxia and intention tremor should be screened for the FMR1 mutation, especially if these signs are accompanied by parkinsonism, autonomic dysfunction, or cognitive decline, regardless of family history.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k#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/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/14747503
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k#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/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
http://purl.org/dc/terms/created
2017-10-17T13:12:48+02:00
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP412725.RAZDjap733DN8CVAny_b9UoHF0eCpJ1mGnQlutnxyFJ4k
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