@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:NP553334.RAbrUoK26N8A_-7ru3J320_wIo5T2h28Zm-GQfcKHjT4A130_head { this: np:hasAssertion dgn-np:NP553334.RAbrUoK26N8A_-7ru3J320_wIo5T2h28Zm-GQfcKHjT4A130_assertion; np:hasProvenance dgn-np:NP553334.RAbrUoK26N8A_-7ru3J320_wIo5T2h28Zm-GQfcKHjT4A130_provenance; np:hasPublicationInfo dgn-np:NP553334.RAbrUoK26N8A_-7ru3J320_wIo5T2h28Zm-GQfcKHjT4A130_publicationInfo; a np:Nanopublication . dgn-np:NP553334.RAbrUoK26N8A_-7ru3J320_wIo5T2h28Zm-GQfcKHjT4A130_assertion a np:Assertion . dgn-np:NP553334.RAbrUoK26N8A_-7ru3J320_wIo5T2h28Zm-GQfcKHjT4A130_provenance a np:Provenance . dgn-np:NP553334.RAbrUoK26N8A_-7ru3J320_wIo5T2h28Zm-GQfcKHjT4A130_publicationInfo a np:PublicationInfo . } dgn-np:NP553334.RAbrUoK26N8A_-7ru3J320_wIo5T2h28Zm-GQfcKHjT4A130_assertion { miriam-gene:4221 a ncit:C16612 . lld:C0030297 a ncit:C7057 . dgn-gda:DGNee34b5723c399c3190276767415d877a sio:SIO_000628 miriam-gene:4221, lld:C0030297; a sio:SIO_001121 . } dgn-np:NP553334.RAbrUoK26N8A_-7ru3J320_wIo5T2h28Zm-GQfcKHjT4A130_provenance { dgn-np:NP553334.RAbrUoK26N8A_-7ru3J320_wIo5T2h28Zm-GQfcKHjT4A130_assertion dcterms:description "[Individuals with at least one typical endocrine tumour and at least one of the following: 1) a first-degree relative with a major endocrine tumor; 2) an age of onset less than 30 yr; and/or 3) multiple pancreatic tumors/parathyroid hyperplasia were most likely to harbor a mutation; thus these patients should be screened for MEN1 mutations.]. 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:17623761; 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:NP553334.RAbrUoK26N8A_-7ru3J320_wIo5T2h28Zm-GQfcKHjT4A130_publicationInfo { this: dcterms:created "2015-08-25T14:43:07+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 "v3.0.0.0" . dgn-void:disgenetv3.0rdf pav:version "v3.0.0" . }