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<http://rdf.disgenet.org/gene-disease-association.ttl#DGN24f74b4bb8d59f8d694ce19ec3d49c78> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0001973> <http://rdf.disgenet.org/nanopublications.trig#NP338892.RATg8MngE11vW9Ps6uc_VDELWAlUvvAlVZKN2ypEnBU_c130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGN24f74b4bb8d59f8d694ce19ec3d49c78> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001121> <http://rdf.disgenet.org/nanopublications.trig#NP338892.RATg8MngE11vW9Ps6uc_VDELWAlUvvAlVZKN2ypEnBU_c130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP338892.RATg8MngE11vW9Ps6uc_VDELWAlUvvAlVZKN2ypEnBU_c130_assertion> <http://purl.org/dc/terms/description> "[Numerous SNPs in ADH genes showed association with AD, including one marker in the coding region of ADH1C (rs1693482 in exon6, Ile271Gln).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP338892.RATg8MngE11vW9Ps6uc_VDELWAlUvvAlVZKN2ypEnBU_c130_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#NP338892.RATg8MngE11vW9Ps6uc_VDELWAlUvvAlVZKN2ypEnBU_c130_provenance> .
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