@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:NP1304172.RA5w6T5BS2VT7Q0UMyuZRp_7veH0kQW93tUiinUg0L7Sw130_head { this: np:hasAssertion dgn-np:NP1304172.RA5w6T5BS2VT7Q0UMyuZRp_7veH0kQW93tUiinUg0L7Sw130_assertion; np:hasProvenance dgn-np:NP1304172.RA5w6T5BS2VT7Q0UMyuZRp_7veH0kQW93tUiinUg0L7Sw130_provenance; np:hasPublicationInfo dgn-np:NP1304172.RA5w6T5BS2VT7Q0UMyuZRp_7veH0kQW93tUiinUg0L7Sw130_publicationInfo; a np:Nanopublication . dgn-np:NP1304172.RA5w6T5BS2VT7Q0UMyuZRp_7veH0kQW93tUiinUg0L7Sw130_assertion a np:Assertion . dgn-np:NP1304172.RA5w6T5BS2VT7Q0UMyuZRp_7veH0kQW93tUiinUg0L7Sw130_provenance a np:Provenance . dgn-np:NP1304172.RA5w6T5BS2VT7Q0UMyuZRp_7veH0kQW93tUiinUg0L7Sw130_publicationInfo a np:PublicationInfo . } dgn-np:NP1304172.RA5w6T5BS2VT7Q0UMyuZRp_7veH0kQW93tUiinUg0L7Sw130_assertion { miriam-gene:2629 a ncit:C16612 . lld:C1961835 a ncit:C7057 . dgn-gda:DGN7f9852687c1d73e551aca992588d113b sio:SIO_000628 miriam-gene:2629, lld:C1961835; a sio:SIO_001121 . } dgn-np:NP1304172.RA5w6T5BS2VT7Q0UMyuZRp_7veH0kQW93tUiinUg0L7Sw130_provenance { dgn-np:NP1304172.RA5w6T5BS2VT7Q0UMyuZRp_7veH0kQW93tUiinUg0L7Sw130_assertion dcterms:description "[These kinetic, immunologic, and thermostability studies indicated that 1) type 1 Gaucher disease is biochemically heterogeneous and results from at least four distinct allelic acid beta-glucosidase mutations that alter enzyme structure and/or function, 2) neuronopathic and non-Jewish non-neuronopathic phenotypes cannot be distinguished reliably by kinetic analyses alone, and 3) the Ashkenazi type 1 Gaucher disease results from a unique mutation that alters a specific active site domain of acid beta-glucosidase.]. 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:3927728; 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:NP1304172.RA5w6T5BS2VT7Q0UMyuZRp_7veH0kQW93tUiinUg0L7Sw130_publicationInfo { this: dcterms:created "2016-05-13T12:51:37+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" . }