@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:NP68117.RAJQT39-yU9vH8FrEgShhuw_2IiJV6qK2MmUUvOgWHMlc130_head { this: np:hasAssertion dgn-np:NP68117.RAJQT39-yU9vH8FrEgShhuw_2IiJV6qK2MmUUvOgWHMlc130_assertion; np:hasProvenance dgn-np:NP68117.RAJQT39-yU9vH8FrEgShhuw_2IiJV6qK2MmUUvOgWHMlc130_provenance; np:hasPublicationInfo dgn-np:NP68117.RAJQT39-yU9vH8FrEgShhuw_2IiJV6qK2MmUUvOgWHMlc130_publicationInfo; a np:Nanopublication . dgn-np:NP68117.RAJQT39-yU9vH8FrEgShhuw_2IiJV6qK2MmUUvOgWHMlc130_assertion a np:Assertion . dgn-np:NP68117.RAJQT39-yU9vH8FrEgShhuw_2IiJV6qK2MmUUvOgWHMlc130_provenance a np:Provenance . dgn-np:NP68117.RAJQT39-yU9vH8FrEgShhuw_2IiJV6qK2MmUUvOgWHMlc130_publicationInfo a np:PublicationInfo . } dgn-np:NP68117.RAJQT39-yU9vH8FrEgShhuw_2IiJV6qK2MmUUvOgWHMlc130_assertion { miriam-gene:356 a ncit:C16612 . lld:C0151449 a ncit:C7057 . dgn-gda:DGN29bf91f6213bbbdc89f46d5852580513 sio:SIO_000628 miriam-gene:356, lld:C0151449; a sio:SIO_001122 . } dgn-np:NP68117.RAJQT39-yU9vH8FrEgShhuw_2IiJV6qK2MmUUvOgWHMlc130_provenance { dgn-np:NP68117.RAJQT39-yU9vH8FrEgShhuw_2IiJV6qK2MmUUvOgWHMlc130_assertion dcterms:description "[ We describe the positions and frequencies of several polymorphisms in the genes encoding Fas and FasL in patients with primary SS. None caused any amino acid change. Three Fas alleles, of which one is located in the promoter area, showed significant alth]. 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:11036836; 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:NP68117.RAJQT39-yU9vH8FrEgShhuw_2IiJV6qK2MmUUvOgWHMlc130_publicationInfo { this: dcterms:created "2016-05-13T12:42:19+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" . }