@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:NP354228.RAdQSdVO5dJrW0_z-9mX8t9D4ZFVUmuwdMpwkIM1x1dVI130_head { this: np:hasAssertion dgn-np:NP354228.RAdQSdVO5dJrW0_z-9mX8t9D4ZFVUmuwdMpwkIM1x1dVI130_assertion; np:hasProvenance dgn-np:NP354228.RAdQSdVO5dJrW0_z-9mX8t9D4ZFVUmuwdMpwkIM1x1dVI130_provenance; np:hasPublicationInfo dgn-np:NP354228.RAdQSdVO5dJrW0_z-9mX8t9D4ZFVUmuwdMpwkIM1x1dVI130_publicationInfo; a np:Nanopublication . dgn-np:NP354228.RAdQSdVO5dJrW0_z-9mX8t9D4ZFVUmuwdMpwkIM1x1dVI130_assertion a np:Assertion . dgn-np:NP354228.RAdQSdVO5dJrW0_z-9mX8t9D4ZFVUmuwdMpwkIM1x1dVI130_provenance a np:Provenance . dgn-np:NP354228.RAdQSdVO5dJrW0_z-9mX8t9D4ZFVUmuwdMpwkIM1x1dVI130_publicationInfo a np:PublicationInfo . } dgn-np:NP354228.RAdQSdVO5dJrW0_z-9mX8t9D4ZFVUmuwdMpwkIM1x1dVI130_assertion { miriam-gene:5378 a ncit:C16612 . lld:C0079731 a ncit:C7057 . dgn-gda:DGN032a2313dbc74fdddf20c537e4014944 sio:SIO_000628 miriam-gene:5378, lld:C0079731; a sio:SIO_001121 . } dgn-np:NP354228.RAdQSdVO5dJrW0_z-9mX8t9D4ZFVUmuwdMpwkIM1x1dVI130_provenance { dgn-np:NP354228.RAdQSdVO5dJrW0_z-9mX8t9D4ZFVUmuwdMpwkIM1x1dVI130_assertion dcterms:description "[The hMSH2 transcript was present in all cases of lymphoma, while the expression of hMLH1 and hPMS1 was significantly low in some large B-cell lymphomas (four and five out of 14 cases, respectively) and in mantle cell lymphomas of the blastoid type (two out of two cases).]. 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:11999575; 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:NP354228.RAdQSdVO5dJrW0_z-9mX8t9D4ZFVUmuwdMpwkIM1x1dVI130_publicationInfo { this: dcterms:created "2016-05-13T12:44:26+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" . }