@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:NP84426.RApXtlrpkMIQt1w3lalwHDdwu_E4MpqjaSEY7qKDZpPRM130_head { this: np:hasAssertion dgn-np:NP84426.RApXtlrpkMIQt1w3lalwHDdwu_E4MpqjaSEY7qKDZpPRM130_assertion; np:hasProvenance dgn-np:NP84426.RApXtlrpkMIQt1w3lalwHDdwu_E4MpqjaSEY7qKDZpPRM130_provenance; np:hasPublicationInfo dgn-np:NP84426.RApXtlrpkMIQt1w3lalwHDdwu_E4MpqjaSEY7qKDZpPRM130_publicationInfo; a np:Nanopublication . dgn-np:NP84426.RApXtlrpkMIQt1w3lalwHDdwu_E4MpqjaSEY7qKDZpPRM130_assertion a np:Assertion . dgn-np:NP84426.RApXtlrpkMIQt1w3lalwHDdwu_E4MpqjaSEY7qKDZpPRM130_provenance a np:Provenance . dgn-np:NP84426.RApXtlrpkMIQt1w3lalwHDdwu_E4MpqjaSEY7qKDZpPRM130_publicationInfo a np:PublicationInfo . } dgn-np:NP84426.RApXtlrpkMIQt1w3lalwHDdwu_E4MpqjaSEY7qKDZpPRM130_assertion { miriam-gene:4221 a ncit:C16612 . lld:C0027662 a ncit:C7057 . dgn-gda:DGNcc3ecb1775b80ae4a0389391b5355e1b sio:SIO_000628 miriam-gene:4221, lld:C0027662; a sio:SIO_001122 . } dgn-np:NP84426.RApXtlrpkMIQt1w3lalwHDdwu_E4MpqjaSEY7qKDZpPRM130_provenance { dgn-np:NP84426.RApXtlrpkMIQt1w3lalwHDdwu_E4MpqjaSEY7qKDZpPRM130_assertion dcterms:description "[In contrast to a previous report, we found that MEN1 phenocopy patients are not necessarily older than probands of familial MEN1. Phenotypic expression of such patients is variable, thus differentiation of familial MEN1 and MEN1 phenocopy cannot be made b]. 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:15034196; prov:wasDerivedFrom dgn-void:gad-20150221; prov:wasGeneratedBy eco:ECO_0000203 . dgn-void:gad-20150221 pav:importedOn "2015-02-21"^^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:NP84426.RApXtlrpkMIQt1w3lalwHDdwu_E4MpqjaSEY7qKDZpPRM130_publicationInfo { this: dcterms:created "2016-05-13T12:42:26+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" . }