@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:NP691425.RAHkd1VPfK_T_WOx6b7dxf2X-DMG21j8PTtxVGdLCaBwU130_head { this: np:hasAssertion dgn-np:NP691425.RAHkd1VPfK_T_WOx6b7dxf2X-DMG21j8PTtxVGdLCaBwU130_assertion; np:hasProvenance dgn-np:NP691425.RAHkd1VPfK_T_WOx6b7dxf2X-DMG21j8PTtxVGdLCaBwU130_provenance; np:hasPublicationInfo dgn-np:NP691425.RAHkd1VPfK_T_WOx6b7dxf2X-DMG21j8PTtxVGdLCaBwU130_publicationInfo; a np:Nanopublication . dgn-np:NP691425.RAHkd1VPfK_T_WOx6b7dxf2X-DMG21j8PTtxVGdLCaBwU130_assertion a np:Assertion . dgn-np:NP691425.RAHkd1VPfK_T_WOx6b7dxf2X-DMG21j8PTtxVGdLCaBwU130_provenance a np:Provenance . dgn-np:NP691425.RAHkd1VPfK_T_WOx6b7dxf2X-DMG21j8PTtxVGdLCaBwU130_publicationInfo a np:PublicationInfo . } dgn-np:NP691425.RAHkd1VPfK_T_WOx6b7dxf2X-DMG21j8PTtxVGdLCaBwU130_assertion { miriam-gene:2312 a ncit:C16612 . lld:C0004096 a ncit:C7057 . dgn-gda:DGNff95b180db1d6c8c94625fc7ea841fd8 sio:SIO_000628 miriam-gene:2312, lld:C0004096; a sio:SIO_001121 . } dgn-np:NP691425.RAHkd1VPfK_T_WOx6b7dxf2X-DMG21j8PTtxVGdLCaBwU130_provenance { dgn-np:NP691425.RAHkd1VPfK_T_WOx6b7dxf2X-DMG21j8PTtxVGdLCaBwU130_assertion dcterms:description "[The identification of mutations in the barrier protein filaggrin as conferring major susceptibility to atopic dermatitis and atopic dermatitis related asthma has reconfigured our understanding of disease mechanisms and highlights the importance of epidermal barrier disruption as a primary event in the disease.]. 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:18769192; 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:NP691425.RAHkd1VPfK_T_WOx6b7dxf2X-DMG21j8PTtxVGdLCaBwU130_publicationInfo { this: dcterms:created "2016-05-13T12:46:58+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" . }