@prefix this: . @prefix rdfs: . @prefix xsd: . @prefix sio: . @prefix ncit: . @prefix lld: . @prefix miriam-gene: . @prefix miriam-pubmed: . @prefix eco: . @prefix wi: . @prefix prov: . @prefix pav: . @prefix prv: . @prefix dcterms: . @prefix np: . @prefix dgn-np: . @prefix dgn-gda: . @prefix dgn-void: . dgn-np:NP1369660.RAiw_uGvpZGuQT6Ev3fQddRbF6SdK7Ut012Q7pnFPHkEU130_head { this: np:hasAssertion dgn-np:NP1369660.RAiw_uGvpZGuQT6Ev3fQddRbF6SdK7Ut012Q7pnFPHkEU130_assertion; np:hasProvenance dgn-np:NP1369660.RAiw_uGvpZGuQT6Ev3fQddRbF6SdK7Ut012Q7pnFPHkEU130_provenance; np:hasPublicationInfo dgn-np:NP1369660.RAiw_uGvpZGuQT6Ev3fQddRbF6SdK7Ut012Q7pnFPHkEU130_publicationInfo; a np:Nanopublication . dgn-np:NP1369660.RAiw_uGvpZGuQT6Ev3fQddRbF6SdK7Ut012Q7pnFPHkEU130_assertion a np:Assertion . dgn-np:NP1369660.RAiw_uGvpZGuQT6Ev3fQddRbF6SdK7Ut012Q7pnFPHkEU130_provenance a np:Provenance . dgn-np:NP1369660.RAiw_uGvpZGuQT6Ev3fQddRbF6SdK7Ut012Q7pnFPHkEU130_publicationInfo a np:PublicationInfo . } dgn-np:NP1369660.RAiw_uGvpZGuQT6Ev3fQddRbF6SdK7Ut012Q7pnFPHkEU130_assertion { miriam-gene:472 a ncit:C16612 . lld:C0678222 a ncit:C7057 . dgn-gda:DGNd97cad1228895b7494e79ac8edbcd822 sio:SIO_000628 miriam-gene:472, lld:C0678222; a sio:SIO_001121 . } dgn-np:NP1369660.RAiw_uGvpZGuQT6Ev3fQddRbF6SdK7Ut012Q7pnFPHkEU130_provenance { dgn-np:NP1369660.RAiw_uGvpZGuQT6Ev3fQddRbF6SdK7Ut012Q7pnFPHkEU130_assertion dcterms:description "[We present a simple and rapid polymerase chain reaction (PCR)-based assay for this dimorphism that should be useful to trace the inheritance of ATM alleles in ataxia telangiectasia and breast cancer families and to study loss of heterozygosity in primary tumours.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en; wi:evidence dgn-void:source_evidence_literature; sio:SIO_000772 miriam-pubmed:9076718; prov:wasDerivedFrom dgn-void:befree-2016; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-2016 pav:importedOn "2016-02-19"^^xsd:date . dgn-void:source_evidence_literature a eco:ECO_0000212; rdfs:comment "Gene-disease associations inferred from text-mining the literature."@en; rdfs:label "DisGeNET evidence - LITERATURE"@en . } dgn-np:NP1369660.RAiw_uGvpZGuQT6Ev3fQddRbF6SdK7Ut012Q7pnFPHkEU130_publicationInfo { this: dcterms:created "2016-05-13T12:52:07+02:00"^^xsd:dateTime; dcterms:rights ; dcterms:rightsHolder dgn-void:IBIGroup; dcterms:subject sio:SIO_000983; prv:usedData dgn-void:disgenetv3.0rdf; pav:authoredBy , , , , ; pav:createdBy ; pav:version "v4.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v4.0.0" . }