@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:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_head { this: np:hasAssertion dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_assertion; np:hasProvenance dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_provenance; np:hasPublicationInfo dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_publicationInfo; a np:Nanopublication . dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_assertion a np:Assertion . dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_provenance a np:Provenance . dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_publicationInfo a np:PublicationInfo . } dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_assertion { miriam-gene:999 a ncit:C16612 . lld:C0036631 a ncit:C7057 . dgn-gda:DGNc1111f547d69648f76b882af5265b75f sio:SIO_000628 miriam-gene:999, lld:C0036631; a sio:SIO_001121 . } dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_provenance { dgn-np:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_assertion dcterms:description "[Occurrence of structural genetic alterations was analyzed in 18 seminomas and 22 non-seminomas for genes involved in the malignant tumour phenotype: cadherin 1, Type 1, E-cadherin (Epithelial), CDH1; adenomatous polyposis coli, APC; NME/NM23 nucleoside diphosphate kinase 1, NME1; tumour protein P53, TP53; cyclin-dependent kinase inhibitor 2A, CDKN2A; retinoblastoma 1, RB1; RAD51 recombinase, RAD51; mutS homolog 2, MSH2; MutL homolog 1, MLH1; breast cancer 1, early onset, BRCA1; BCL2-Associated X Protein, BAX; ATP-Binding Cassette, Sub-Family G (WHITE), Member 2, ABCG2.]. 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:25075023; prov:wasDerivedFrom dgn-void:befree-20150227; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:befree-20150227 pav:importedOn "2015-02-27"^^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:NP299474.RASpUrAbzHLcF_7czBOHMQtgfmg7yvdwxbh8kgjWxwGD8130_publicationInfo { this: dcterms:created "2015-08-25T14:40:32+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }