@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ
> .
@prefix rdfs: <
http://www.w3.org/2000/01/rdf-schema#
> .
@prefix xsd: <
http://www.w3.org/2001/XMLSchema#
> .
@prefix sio: <
http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
@prefix lld: <
http://linkedlifedata.com/resource/umls/id/
> .
@prefix miriam-gene: <
http://identifiers.org/ncbigene/
> .
@prefix miriam-pubmed: <
http://identifiers.org/pubmed/
> .
@prefix eco: <
http://purl.obolibrary.org/obo/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@prefix prv: <
http://purl.org/net/provenance/ns#
> .
@prefix dcterms: <
http://purl.org/dc/terms/
> .
@prefix np: <
http://www.nanopub.org/nschema#
> .
@prefix dgn-np: <
http://rdf.disgenet.org/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_head
{
this:
np:hasAssertion
dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_assertion
;
np:hasProvenance
dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_assertion
a
np:Assertion
.
dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_provenance
a
np:Provenance
.
dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0524620
a
ncit:C7057
.
dgn-gda:DGN2ba9847d25513249f930aed827941fb2
sio:SIO_000628
miriam-gene:4000
,
lld:C0524620
;
a
sio:SIO_001121
.
}
dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_provenance
{
dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_assertion
dcterms:description
"[One form of lipodystrophy, namely Dunnigan-type familial partial lipodystrophy (FPLD) was shown to result from mutations in the LMNA gene, which encodes nuclear lamins A and C. Although the relationship between the mutations in the nuclear envelope and insulin resistance is unclear at present, these findings might eventually be shown to have relevance for the common insulin resistance syndrome and for drug-associated lipodystrophies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
;
sio:SIO_000772
miriam-pubmed:11286783
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
xsd:date
.
dgn-void:source_evidence_literature
a
eco:ECO_0000212
;
rdfs:comment
"Gene-disease associations inferred from text-mining the literature."@en ;
rdfs:label
"DisGeNET evidence - LITERATURE"@en .
}
dgn-np:NP371953.RAX-OC3D4HPvOVsd8ZpP_0jcDjPV0xgG9CXa5b7546HLQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:38+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
;
dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
<
http://orcid.org/0000-0001-5999-6269
> , <
http://orcid.org/0000-0002-7534-7661
> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}