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<http://identifiers.org/ncbigene/4204> <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#NP54798.RAEm3X-G7bhV_31DYX8DyaNx2HrvEyTwqgI1KwldiXlQI130_assertion> .
<http://linkedlifedata.com/resource/umls/id/C0035372> <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#NP54798.RAEm3X-G7bhV_31DYX8DyaNx2HrvEyTwqgI1KwldiXlQI130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGNcda447ab313b8a8365cecd33a736582d> <http://semanticscience.org/resource/SIO_000628> <http://identifiers.org/ncbigene/4204> <http://rdf.disgenet.org/nanopublications.trig#NP54798.RAEm3X-G7bhV_31DYX8DyaNx2HrvEyTwqgI1KwldiXlQI130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGNcda447ab313b8a8365cecd33a736582d> <http://semanticscience.org/resource/SIO_000628> <http://linkedlifedata.com/resource/umls/id/C0035372> <http://rdf.disgenet.org/nanopublications.trig#NP54798.RAEm3X-G7bhV_31DYX8DyaNx2HrvEyTwqgI1KwldiXlQI130_assertion> .
<http://rdf.disgenet.org/gene-disease-association.ttl#DGNcda447ab313b8a8365cecd33a736582d> <http://www.w3.org/1999/02/22-rdf-syntax-ns#type> <http://semanticscience.org/resource/SIO_001122> <http://rdf.disgenet.org/nanopublications.trig#NP54798.RAEm3X-G7bhV_31DYX8DyaNx2HrvEyTwqgI1KwldiXlQI130_assertion> .
<http://rdf.disgenet.org/nanopublications.trig#NP54798.RAEm3X-G7bhV_31DYX8DyaNx2HrvEyTwqgI1KwldiXlQI130_assertion> <http://purl.org/dc/terms/description> "[RTT females with the T158M missense mutation are often atypical with mainly behavioral characteristics in infancy and childhood but become classic RTT in adolescence after a slower, protracted course.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en <http://rdf.disgenet.org/nanopublications.trig#NP54798.RAEm3X-G7bhV_31DYX8DyaNx2HrvEyTwqgI1KwldiXlQI130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP54798.RAEm3X-G7bhV_31DYX8DyaNx2HrvEyTwqgI1KwldiXlQI130_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#NP54798.RAEm3X-G7bhV_31DYX8DyaNx2HrvEyTwqgI1KwldiXlQI130_provenance> .
<http://rdf.disgenet.org/nanopublications.trig#NP54798.RAEm3X-G7bhV_31DYX8DyaNx2HrvEyTwqgI1KwldiXlQI130_assertion> <http://semanticscience.org/resource/SIO_000772> <http://identifiers.org/pubmed/19133691> <http://rdf.disgenet.org/nanopublications.trig#NP54798.RAEm3X-G7bhV_31DYX8DyaNx2HrvEyTwqgI1KwldiXlQI130_provenance> .
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<http://rdf.disgenet.org/v2.1.0/void.ttl#gad-20130706> <http://purl.org/pav/2.0/importedOn> "2013-07-06"^^<http://www.w3.org/2001/XMLSchema#date> <http://rdf.disgenet.org/nanopublications.trig#NP54798.RAEm3X-G7bhV_31DYX8DyaNx2HrvEyTwqgI1KwldiXlQI130_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#NP54798.RAEm3X-G7bhV_31DYX8DyaNx2HrvEyTwqgI1KwldiXlQI130_provenance> .
<http://rdf.disgenet.org/v2.1.0/void.ttl#source_evidence_literature> <http://www.w3.org/2000/01/rdf-schema#label> "DisGeNET evidence - LITERATURE"@en <http://rdf.disgenet.org/nanopublications.trig#NP54798.RAEm3X-G7bhV_31DYX8DyaNx2HrvEyTwqgI1KwldiXlQI130_provenance> .
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