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<http://identifiers.org/ncbigene/7248> <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#NP201964.RAdALjbcuf29gThdT2hgV4fwJxvuEWNw1MKdjm6hyruE0130_assertion> .
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<http://rdf.disgenet.org/gene-disease-association.ttl#DGNe48bdf57f837e255395771a3322fe2d5> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001121> <http://rdf.disgenet.org/nanopublications.trig#NP201964.RAdALjbcuf29gThdT2hgV4fwJxvuEWNw1MKdjm6hyruE0130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP201964.RAdALjbcuf29gThdT2hgV4fwJxvuEWNw1MKdjm6hyruE0130_assertion> <http://purl.org/dc/terms/description> "[Each tumour was assessed for allele loss at ten microsatellite markers which map close to known or putative tumour-suppressor genes: APC (5q21-q22); DCC (18q21.1); 1p35-p36; p16 (9p21); 22q; 8p; E-cadherin (16q22.1); beta-catenin (3p22-p21.3); RB1 (13q14.1-q14.2); and HLA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP201964.RAdALjbcuf29gThdT2hgV4fwJxvuEWNw1MKdjm6hyruE0130_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#NP201964.RAdALjbcuf29gThdT2hgV4fwJxvuEWNw1MKdjm6hyruE0130_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#NP201964.RAdALjbcuf29gThdT2hgV4fwJxvuEWNw1MKdjm6hyruE0130_provenance> .
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