@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:NP988057.RArxL682DhL_8D-2vISLpVJZYUahDPnw1VT0CbUTSUrrw130_head { this: np:hasAssertion dgn-np:NP988057.RArxL682DhL_8D-2vISLpVJZYUahDPnw1VT0CbUTSUrrw130_assertion; np:hasProvenance dgn-np:NP988057.RArxL682DhL_8D-2vISLpVJZYUahDPnw1VT0CbUTSUrrw130_provenance; np:hasPublicationInfo dgn-np:NP988057.RArxL682DhL_8D-2vISLpVJZYUahDPnw1VT0CbUTSUrrw130_publicationInfo; a np:Nanopublication . dgn-np:NP988057.RArxL682DhL_8D-2vISLpVJZYUahDPnw1VT0CbUTSUrrw130_assertion a np:Assertion . dgn-np:NP988057.RArxL682DhL_8D-2vISLpVJZYUahDPnw1VT0CbUTSUrrw130_provenance a np:Provenance . dgn-np:NP988057.RArxL682DhL_8D-2vISLpVJZYUahDPnw1VT0CbUTSUrrw130_publicationInfo a np:PublicationInfo . } dgn-np:NP988057.RArxL682DhL_8D-2vISLpVJZYUahDPnw1VT0CbUTSUrrw130_assertion { miriam-gene:2548 a ncit:C16612 . lld:C0085078 a ncit:C7057 . dgn-gda:DGN7e0838b3d1de11870b5ed2537a957f67 sio:SIO_000628 miriam-gene:2548, lld:C0085078; a sio:SIO_001121 . } dgn-np:NP988057.RArxL682DhL_8D-2vISLpVJZYUahDPnw1VT0CbUTSUrrw130_provenance { dgn-np:NP988057.RArxL682DhL_8D-2vISLpVJZYUahDPnw1VT0CbUTSUrrw130_assertion dcterms:description "[Pompe disease (Glycogen storage disease type II, GSD II, acid alpha-glucosidase deficiency, acid maltase deficiency, OMIM # 232300) is an autosomal-recessive lysosomal storage disorder due to a deficiency of acid alpha-glucosidase (GAA, acid maltase, EC 3.2.1.20, Swiss-Prot P10253).]. 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:22676651; 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:NP988057.RArxL682DhL_8D-2vISLpVJZYUahDPnw1VT0CbUTSUrrw130_publicationInfo { this: dcterms:created "2016-05-13T12:49:13+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" . }