@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:NP1081073.RALjfNwFbwY2dJXFyr-JwDHLgigk9ooPoN8W2h2iHfbAw130_head { this: np:hasAssertion dgn-np:NP1081073.RALjfNwFbwY2dJXFyr-JwDHLgigk9ooPoN8W2h2iHfbAw130_assertion; np:hasProvenance dgn-np:NP1081073.RALjfNwFbwY2dJXFyr-JwDHLgigk9ooPoN8W2h2iHfbAw130_provenance; np:hasPublicationInfo dgn-np:NP1081073.RALjfNwFbwY2dJXFyr-JwDHLgigk9ooPoN8W2h2iHfbAw130_publicationInfo; a np:Nanopublication . dgn-np:NP1081073.RALjfNwFbwY2dJXFyr-JwDHLgigk9ooPoN8W2h2iHfbAw130_assertion a np:Assertion . dgn-np:NP1081073.RALjfNwFbwY2dJXFyr-JwDHLgigk9ooPoN8W2h2iHfbAw130_provenance a np:Provenance . dgn-np:NP1081073.RALjfNwFbwY2dJXFyr-JwDHLgigk9ooPoN8W2h2iHfbAw130_publicationInfo a np:PublicationInfo . } dgn-np:NP1081073.RALjfNwFbwY2dJXFyr-JwDHLgigk9ooPoN8W2h2iHfbAw130_assertion { miriam-gene:4598 a ncit:C16612 . lld:C0031069 a ncit:C7057 . dgn-gda:DGN4be53d63239179517aa4a2e064ff4003 sio:SIO_000628 miriam-gene:4598, lld:C0031069; a sio:SIO_001121 . } dgn-np:NP1081073.RALjfNwFbwY2dJXFyr-JwDHLgigk9ooPoN8W2h2iHfbAw130_provenance { dgn-np:NP1081073.RALjfNwFbwY2dJXFyr-JwDHLgigk9ooPoN8W2h2iHfbAw130_assertion dcterms:description "[The autoinflammatory diseases can be grouped based on clinical findings: 1. the three classic hereditary periodic fever syndromes, familial Mediterranean Fever (FMF); TNF receptor associated periodic syndrome (TRAPS); and mevalonate kinase deficiency/hyperimmunoglobulinemia D and periodic fever syndrome (HIDS); 2. the cryopyrin associated periodic syndromes (CAPS), comprising familial cold autoinflammatory syndrome (FCAS), Muckle-Wells syndrome (MWS) and neonatal-onset multisystem inflammatory disease (NOMID) or CINCA, and; 3. pediatric granulomatous arthritis (PGA); 4. disorders presenting with skin pustules, including deficiency of interleukin 1 receptor antagonist (DIRA); Majeed syndrome; pyogenic arthritis, pyoderma gangrenosum and acne (PAPA) syndrome; deficiency of interleukin 36 receptor antagonist (DITRA); CARD14 mediated psoriasis (CAMPS), and early-onset inflammatory bowel diseases (EO-IBD); 5. inflammatory disorders caused by mutations in proteasome components, the proteasome associated autoinflammatory syndromes (PRAAS) and 6. very rare conditions presenting with autoinflammation and immunodeficiency.]. 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:23711932; 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:NP1081073.RALjfNwFbwY2dJXFyr-JwDHLgigk9ooPoN8W2h2iHfbAw130_publicationInfo { this: dcterms:created "2016-05-13T12:49:56+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" . }