http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss#head http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss#assertion http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss#provenance http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss#assertion http://rdf.disgenet.org/resource/gda/DGN1e7d4822a6c240f9fd122ea7d7316df1 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/8398 http://rdf.disgenet.org/resource/gda/DGN1e7d4822a6c240f9fd122ea7d7316df1 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0270724 http://rdf.disgenet.org/resource/gda/DGN1e7d4822a6c240f9fd122ea7d7316df1 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001122 http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss#provenance http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss#assertion http://purl.org/dc/terms/description [PLA2G6 mutations are associated with infantile neuroaxonal dystrophy and have been reported previously to cause early cerebellar signs, and the syndrome was classified as neurodegeneration with brain iron accumulation (type 2).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss#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/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/18570303 http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss#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/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss http://purl.org/dc/terms/created 2017-10-17T13:17:28+02:00 http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1143927.RAUNhfVy-SQbkbP_SHGEiEKx26-2nVPnKtVIZMpCjKlss 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