http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY#head
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
http://www.nanopub.org/nschema#hasAssertion
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY#assertion
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
http://www.nanopub.org/nschema#hasProvenance
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY#provenance
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
http://www.nanopub.org/nschema#hasPublicationInfo
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://www.nanopub.org/nschema#Nanopublication
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY#assertion
http://rdf.disgenet.org/resource/gda/DGNb244f9b870262a5a93e610b7aa4426d3
http://semanticscience.org/resource/SIO_000628
http://identifiers.org/ncbigene/4000
http://rdf.disgenet.org/resource/gda/DGNb244f9b870262a5a93e610b7aa4426d3
http://semanticscience.org/resource/SIO_000628
http://linkedlifedata.com/resource/umls/id/C0878544
http://rdf.disgenet.org/resource/gda/DGNb244f9b870262a5a93e610b7aa4426d3
http://www.w3.org/1999/02/22-rdf-syntax-ns#type
http://semanticscience.org/resource/SIO_001122
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY#provenance
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY#assertion
http://purl.org/dc/terms/description
[Novel genetic defects in the LMNA gene in two families with the Dunnigan variety of familial partial lipodystrophy, cardiac conduction system defects, and other manifestations related to cardiomyopathy suggest the occurrence of a multisystem dystrophy syndrome due to LMNA mutations.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine.
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY#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/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY#assertion
http://semanticscience.org/resource/SIO_000772
http://identifiers.org/pubmed/12015247
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY#assertion
http://www.w3.org/ns/prov#wasDerivedFrom
http://rdf.disgenet.org/v5.0.0/void/BEFREE
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY#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/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY#publicationInfo
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
http://purl.org/dc/terms/created
2017-10-17T13:14:19+02:00
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
http://purl.org/dc/terms/rights
http://opendatacommons.org/licenses/odbl/1.0/
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
http://purl.org/dc/terms/rightsHolder
http://rdf.disgenet.org/v5.0.0/void/IBIGroup
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
http://purl.org/dc/terms/subject
http://semanticscience.org/resource/SIO_000983
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
http://purl.org/net/provenance/ns#usedData
http://rdf.disgenet.org/v5.0.0/void/disgenetv3.0rdf
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0001-5999-6269
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-7534-7661
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0002-9383-528X
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
http://purl.org/pav/authoredBy
http://orcid.org/0000-0003-1244-7654
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
http://purl.org/pav/createdBy
http://orcid.org/0000-0003-0169-8159
http://rdf.disgenet.org/resource/nanopub/NP649714.RAGLrWvvIwEPiqDNbr_gQhIHwh41IGvJz6Aq1VzhdnarY
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