http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI#head http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI#assertion http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI#provenance http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI#assertion http://rdf.disgenet.org/resource/gda/DGN48748c02ef2b9553f52a963e1e9a29ed http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/84947 http://rdf.disgenet.org/resource/gda/DGN48748c02ef2b9553f52a963e1e9a29ed http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C3696376 http://rdf.disgenet.org/resource/gda/DGN48748c02ef2b9553f52a963e1e9a29ed http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI#provenance http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI#assertion http://purl.org/dc/terms/description [A common mitochondrial cause for 3-methylglutaconic aciduria appears to be disruption of the architecture of the mitochondrial membranes, as in Barth syndrome (tafazzin deficiency), Sengers syndrome (acylglycerol kinase deficiency) and MEGDEL syndrome (impaired remodelling of the mitochondrial membrane lipids because of SERAC1 mutations).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/25595726 http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000203 http://rdf.disgenet.org/v5.0.0/void/BEFREE http://purl.org/pav/importedOn 2017-02-19 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000212 http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations inferred from text-mining the literature. http://rdf.disgenet.org/v5.0.0/void/source_evidence_literature http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - LITERATURE http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://purl.org/dc/terms/created 2017-10-17T13:19:00+02:00 http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1388200.RAOzkRZOn426lAygawbrsrAGm-VxnXERjpbZaCaMZ2dyI http://purl.org/pav/version v5.0.0.0 http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://purl.org/pav/version v5.0.0