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<http://rdf.disgenet.org/gene-disease-association.ttl#DGN9195e617e52f9e187cda227d810986cf> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0242383> <http://rdf.disgenet.org/nanopublications.trig#NP593153.RAnoWmRXB1_NNVlaub2evZUXuxywFitGF5_8psFqbCSMU130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN9195e617e52f9e187cda227d810986cf> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001121> <http://rdf.disgenet.org/nanopublications.trig#NP593153.RAnoWmRXB1_NNVlaub2evZUXuxywFitGF5_8psFqbCSMU130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP593153.RAnoWmRXB1_NNVlaub2evZUXuxywFitGF5_8psFqbCSMU130_assertion> <http://purl.org/dc/terms/description> "[We postulated that DNA sequence variation in PPAR gamma (PPARG) co-activator 1 alpha (PPARGC1A), a gene encoding a co-activator of the LCPUFA-sensing PPARG-retinoid X receptor (RXR) transcription complex, may influence neovascularization (NV) in age-related macular degeneration (AMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP593153.RAnoWmRXB1_NNVlaub2evZUXuxywFitGF5_8psFqbCSMU130_provenance> .
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<http://rdf.disgenet.org/v2.1.0/void.ttl#befree-20140225> <http://purl.org/pav/2.0/importedOn> "2014-02-25"^^<http://www.w3.org/2001/XMLSchema#date> <http://rdf.disgenet.org/nanopublications.trig#NP593153.RAnoWmRXB1_NNVlaub2evZUXuxywFitGF5_8psFqbCSMU130_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#NP593153.RAnoWmRXB1_NNVlaub2evZUXuxywFitGF5_8psFqbCSMU130_provenance> .
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