@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:NP652613.RAvVNg9KV-XxZEsjdXngRPNXGLS7RXNdmz5sVvuIc0Lu8130_head { this: np:hasAssertion dgn-np:NP652613.RAvVNg9KV-XxZEsjdXngRPNXGLS7RXNdmz5sVvuIc0Lu8130_assertion; np:hasProvenance dgn-np:NP652613.RAvVNg9KV-XxZEsjdXngRPNXGLS7RXNdmz5sVvuIc0Lu8130_provenance; np:hasPublicationInfo dgn-np:NP652613.RAvVNg9KV-XxZEsjdXngRPNXGLS7RXNdmz5sVvuIc0Lu8130_publicationInfo; a np:Nanopublication . dgn-np:NP652613.RAvVNg9KV-XxZEsjdXngRPNXGLS7RXNdmz5sVvuIc0Lu8130_assertion a np:Assertion . dgn-np:NP652613.RAvVNg9KV-XxZEsjdXngRPNXGLS7RXNdmz5sVvuIc0Lu8130_provenance a np:Provenance . dgn-np:NP652613.RAvVNg9KV-XxZEsjdXngRPNXGLS7RXNdmz5sVvuIc0Lu8130_publicationInfo a np:PublicationInfo . } dgn-np:NP652613.RAvVNg9KV-XxZEsjdXngRPNXGLS7RXNdmz5sVvuIc0Lu8130_assertion { miriam-gene:10892 a ncit:C16612 . lld:C0349532 a ncit:C7057 . dgn-gda:DGN86bb1d371b663331c962e991b2739f02 sio:SIO_000628 miriam-gene:10892, lld:C0349532; a sio:SIO_001121 . } dgn-np:NP652613.RAvVNg9KV-XxZEsjdXngRPNXGLS7RXNdmz5sVvuIc0Lu8130_provenance { dgn-np:NP652613.RAvVNg9KV-XxZEsjdXngRPNXGLS7RXNdmz5sVvuIc0Lu8130_assertion dcterms:description "[In the present study, the frequency of the numeric and structural aberrations of the chromosomes 1, 3, 12, 18 and X and of the MALT1 gene as well as their potential clinical significance were analyzed by using fluorescent in situ hybridization on a tissue microarray containing 257 tissue samples from 203 cases of surgically resected primary gastric lymphomas including 115 cases of MALT lymphomas, 88 cases of diffuse large B-cell lymphomas (DLBCLs, 75 with an associated MALT lymphoma, so-called ex-MALT DLBCL, and 13 de novo), and 54 controls cases of Helicobacter pylori-associated chronic gastritis.]. 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:18234275; 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:NP652613.RAvVNg9KV-XxZEsjdXngRPNXGLS7RXNdmz5sVvuIc0Lu8130_publicationInfo { this: dcterms:created "2016-05-13T12:46:41+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" . }