http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0#head
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0#assertion
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0#provenance
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0#assertion
http://rdf.disgenet.org/resource/gda/DGN03de7e53609ca8681cafbd6294886676
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/8398
http://rdf.disgenet.org/resource/gda/DGN03de7e53609ca8681cafbd6294886676
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C1857747
http://rdf.disgenet.org/resource/gda/DGN03de7e53609ca8681cafbd6294886676
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0#provenance
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0#assertion
http://purl.org/dc/terms/description
[More recently, it was found that mutations in the PLA2G6 gene cause both infantile neuroaxonal dystrophy (INAD) and, more rarely, an atypical neuroaxonal dystrophy that overlaps clinically with other forms of NBIA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0#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/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/18981035
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0#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/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
http://purl.org/dc/terms/created
2017-10-17T13:17:28+02:00
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP1143626.RA3VXcEUNqAj5x5OBYlRyK8hN5LotnMb2MyUkAH7zWda0
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