http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0#head http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 http://www.nanopub.org/nschema#hasAssertion http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0#assertion http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 http://www.nanopub.org/nschema#hasProvenance http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0#provenance http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 http://www.nanopub.org/nschema#hasPublicationInfo http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://www.nanopub.org/nschema#Nanopublication http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0#assertion http://rdf.disgenet.org/resource/gda/DGNf7e3bb47609aea62d2247187b42b7d20 http://semanticscience.org/resource/SIO_000628 http://identifiers.org/ncbigene/9927 http://rdf.disgenet.org/resource/gda/DGNf7e3bb47609aea62d2247187b42b7d20 http://semanticscience.org/resource/SIO_000628 http://linkedlifedata.com/resource/umls/id/C0270921 http://rdf.disgenet.org/resource/gda/DGNf7e3bb47609aea62d2247187b42b7d20 http://www.w3.org/1999/02/22-rdf-syntax-ns#type http://semanticscience.org/resource/SIO_001121 http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0#provenance http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0#assertion http://purl.org/dc/terms/description [This study also demonstrates the value of MFN2 studies in cases of congenital axonal neuropathy, especially in cases of dominant inheritance, severe clinical symptoms or additional symptoms such as optic atrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine. http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0#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/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0#assertion http://semanticscience.org/resource/SIO_000772 http://identifiers.org/pubmed/19889647 http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0#assertion http://www.w3.org/ns/prov#wasDerivedFrom http://rdf.disgenet.org/v5.0.0/void/BEFREE http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0#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/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0#publicationInfo http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 http://purl.org/dc/terms/created 2017-10-17T13:17:50+02:00 http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 http://purl.org/dc/terms/rights http://opendatacommons.org/licenses/odbl/1.0/ http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 http://purl.org/dc/terms/rightsHolder http://rdf.disgenet.org/v5.0.0/void/IBIGroup http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 http://purl.org/dc/terms/subject http://semanticscience.org/resource/SIO_000983 http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 http://purl.org/net/provenance/ns#usedData http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 http://purl.org/pav/authoredBy http://orcid.org/0000-0001-5999-6269 http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-7534-7661 http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 http://purl.org/pav/authoredBy http://orcid.org/0000-0002-9383-528X http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 http://purl.org/pav/authoredBy http://orcid.org/0000-0003-1244-7654 http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 http://purl.org/pav/createdBy http://orcid.org/0000-0003-0169-8159 http://rdf.disgenet.org/resource/nanopub/NP1200229.RA_AL7KohjktNYiGHxcsLv1vtXuSJcbBQK8uy68uVOsV0 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