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<http://identifiers.org/ncbigene/6712> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C16612> <http://rdf.disgenet.org/nanopublications.trig#NP110249.RABpjUXSGDpQVWeAOJllzJBzb_srIAImp--YSanW_LeCQ130_assertion> .
<http://linkedlifedata.com/resource/umls/id/C0087012> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#C7057> <http://rdf.disgenet.org/nanopublications.trig#NP110249.RABpjUXSGDpQVWeAOJllzJBzb_srIAImp--YSanW_LeCQ130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGNb0a82672b6e357e8d8b1f8898b3a7550> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ncbigene/6712> <http://rdf.disgenet.org/nanopublications.trig#NP110249.RABpjUXSGDpQVWeAOJllzJBzb_srIAImp--YSanW_LeCQ130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGNb0a82672b6e357e8d8b1f8898b3a7550> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0087012> <http://rdf.disgenet.org/nanopublications.trig#NP110249.RABpjUXSGDpQVWeAOJllzJBzb_srIAImp--YSanW_LeCQ130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGNb0a82672b6e357e8d8b1f8898b3a7550> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001122> <http://rdf.disgenet.org/nanopublications.trig#NP110249.RABpjUXSGDpQVWeAOJllzJBzb_srIAImp--YSanW_LeCQ130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP110249.RABpjUXSGDpQVWeAOJllzJBzb_srIAImp--YSanW_LeCQ130_assertion> <http://purl.org/dc/terms/description> "[beta-III spectrin (SPTBN2) mutations cause spinocerebellar ataxia type 5 (SCA5) in an 11-generation American kindred descended from President Lincoln's grandparents and two additional families.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP110249.RABpjUXSGDpQVWeAOJllzJBzb_srIAImp--YSanW_LeCQ130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP110249.RABpjUXSGDpQVWeAOJllzJBzb_srIAImp--YSanW_LeCQ130_assertion> <http://purl.org/ontology/wi/core#evidence> <http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://rdf.disgenet.org/nanopublications.trig#NP110249.RABpjUXSGDpQVWeAOJllzJBzb_srIAImp--YSanW_LeCQ130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP110249.RABpjUXSGDpQVWeAOJllzJBzb_srIAImp--YSanW_LeCQ130_assertion> <http://semanticscience.org/resource/SIO_000772> <http://identifiers.org/pubmed/16429157> <http://rdf.disgenet.org/nanopublications.trig#NP110249.RABpjUXSGDpQVWeAOJllzJBzb_srIAImp--YSanW_LeCQ130_provenance> .
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<http://rdf.disgenet.org/v2.1.0/void.ttl#lhgdn-20090331> <http://purl.org/pav/2.0/importedOn> "2009-03-31"^^<http://www.w3.org/2001/XMLSchema#date> <http://rdf.disgenet.org/nanopublications.trig#NP110249.RABpjUXSGDpQVWeAOJllzJBzb_srIAImp--YSanW_LeCQ130_provenance> .
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<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/2000/01/rdf-schema#comment> "Gene-disease associations inferred from text-mining the literature."@en <http://rdf.disgenet.org/nanopublications.trig#NP110249.RABpjUXSGDpQVWeAOJllzJBzb_srIAImp--YSanW_LeCQ130_provenance> .
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