http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM#head http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM#assertion http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM#provenance http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM#assertion http://rdf.disgenet.org/resource/gda/DGN919614483947cd8129c2cf4558c1f390 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/6584 http://rdf.disgenet.org/resource/gda/DGN919614483947cd8129c2cf4558c1f390 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0342788 http://rdf.disgenet.org/resource/gda/DGN919614483947cd8129c2cf4558c1f390 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001121 http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM#provenance http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM#assertion http://purl.org/dc/terms/description [Additional molecular investigations identified two mutations (R254X and IVS3 + 1G > A) in the patient's OCTN2 (SLC22A5) gene, consistent with a diagnosis of primary carnitine deficiency due to carnitine transporter defect.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM#assertion http://purl.org/ontology/wi/core#evidence http://rdf.disgenet.org/v5.0.0/void/source_evidence_curated http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/17703373 http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/CTD_human http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM#assertion http://www.w3.org/ns/prov#wasGeneratedBy http://purl.obolibrary.org/obo/ECO_0000218 http://rdf.disgenet.org/v5.0.0/void/CTD_human http://purl.org/pav/importedOn 2017-01-25 http://rdf.disgenet.org/v5.0.0/void/source_evidence_curated http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://purl.obolibrary.org/obo/ECO_0000205 http://rdf.disgenet.org/v5.0.0/void/source_evidence_curated http://www.w3.org/2000/01/rdf-schema#comment Gene-disease associations manually curated. http://rdf.disgenet.org/v5.0.0/void/source_evidence_curated http://www.w3.org/2000/01/rdf-schema#label DisGeNET evidence - CURATED http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM http://purl.org/dc/terms/created 2017-10-17T13:16:18+02:00 http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP959315.RAeDoNIxW9lrEEYAha0LF3mXbMfDFkff1WmUe-rW0eTIM 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