http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI#head
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI#assertion
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI#provenance
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI#assertion
http://rdf.disgenet.org/resource/gda/DGNca6408dcc58ae04d72bcf407ce78f263
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/6647
http://rdf.disgenet.org/resource/gda/DGNca6408dcc58ae04d72bcf407ce78f263
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C1848922
http://rdf.disgenet.org/resource/gda/DGNca6408dcc58ae04d72bcf407ce78f263
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001121
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI#provenance
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI#assertion
http://purl.org/dc/terms/description
[Genetic mutations have been identified in the major motor neuron diseases, including ALS, spinal muscular atrophy, bulbospinal muscular atrophy (Kennedy's disease), the hereditary spastic paraplegias, and rarer conditions such as GM2 gangliosidosis (hexosaminidase A deficiency).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI#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/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/11460829
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI#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/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
http://purl.org/dc/terms/created
2017-10-17T13:16:22+02:00
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP968660.RAt-IeCjlvTKZHxDt-f5SDQKM9EOGj3nJQZziACvCTCyI
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