http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc#head http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc#assertion http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc#provenance http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc#assertion http://rdf.disgenet.org/resource/gda/DGN6950d88820c1b2af5562fc0410dc9d2c http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/10133 http://rdf.disgenet.org/resource/gda/DGN6950d88820c1b2af5562fc0410dc9d2c http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0002736 http://rdf.disgenet.org/resource/gda/DGN6950d88820c1b2af5562fc0410dc9d2c http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc#provenance http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc#assertion http://purl.org/dc/terms/description [The purpose of this study was to assess the frequency of optineurin (OPTN) mutation in amyotrophic lateral sclerosis (ALS) patients from mainland China, as well as to characterize the relationship between OPTN mutation and clinical phenotypes.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc#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/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/26503823 http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc#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/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc http://purl.org/dc/terms/created 2017-10-17T13:17:53+02:00 http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1207288.RAEUALFGLLQrep4SbPlW-9306Z2CKHrM7F6ZztH1C1LGc 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