@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP539092.RAd03p1QfX3uss15MDErTD1kcExOLHJJccJnNxhr-Bjx8
> .
@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:NP539092.RAd03p1QfX3uss15MDErTD1kcExOLHJJccJnNxhr-Bjx8130_head
{
this:
np:hasAssertion
dgn-np:NP539092.RAd03p1QfX3uss15MDErTD1kcExOLHJJccJnNxhr-Bjx8130_assertion
;
np:hasProvenance
dgn-np:NP539092.RAd03p1QfX3uss15MDErTD1kcExOLHJJccJnNxhr-Bjx8130_provenance
;
np:hasPublicationInfo
dgn-np:NP539092.RAd03p1QfX3uss15MDErTD1kcExOLHJJccJnNxhr-Bjx8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP539092.RAd03p1QfX3uss15MDErTD1kcExOLHJJccJnNxhr-Bjx8130_assertion
a
np:Assertion
.
dgn-np:NP539092.RAd03p1QfX3uss15MDErTD1kcExOLHJJccJnNxhr-Bjx8130_provenance
a
np:Provenance
.
dgn-np:NP539092.RAd03p1QfX3uss15MDErTD1kcExOLHJJccJnNxhr-Bjx8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP539092.RAd03p1QfX3uss15MDErTD1kcExOLHJJccJnNxhr-Bjx8130_assertion
{
miriam-gene:10555
a
ncit:C16612
.
lld:C0023787
a
ncit:C7057
.
dgn-gda:DGN03c4ba66b8cd08d6e6bdec8e7336b376
sio:SIO_000628
miriam-gene:10555
,
lld:C0023787
;
a
sio:SIO_001121
.
}
dgn-np:NP539092.RAd03p1QfX3uss15MDErTD1kcExOLHJJccJnNxhr-Bjx8130_provenance
{
dgn-np:NP539092.RAd03p1QfX3uss15MDErTD1kcExOLHJJccJnNxhr-Bjx8130_assertion
dcterms:description
"[We conducted an open-label prospective study of patients with acquired forms of lipodystrophy and inherited forms of lipodystrophy secondary to mutations in the AGPAT2, SEIPIN (also known as BSCL2), LMNA and PPARgamma (also known as PPARG) genes.]. 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:19727665
;
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:NP539092.RAd03p1QfX3uss15MDErTD1kcExOLHJJccJnNxhr-Bjx8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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" .
}