@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP394302.RA4qtaXGSU6-Wzx-jx47bMKxPPi3BrARxnn-ybwdYXcV8
> .
@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:NP394302.RA4qtaXGSU6-Wzx-jx47bMKxPPi3BrARxnn-ybwdYXcV8130_head
{
this:
np:hasAssertion
dgn-np:NP394302.RA4qtaXGSU6-Wzx-jx47bMKxPPi3BrARxnn-ybwdYXcV8130_assertion
;
np:hasProvenance
dgn-np:NP394302.RA4qtaXGSU6-Wzx-jx47bMKxPPi3BrARxnn-ybwdYXcV8130_provenance
;
np:hasPublicationInfo
dgn-np:NP394302.RA4qtaXGSU6-Wzx-jx47bMKxPPi3BrARxnn-ybwdYXcV8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP394302.RA4qtaXGSU6-Wzx-jx47bMKxPPi3BrARxnn-ybwdYXcV8130_assertion
a
np:Assertion
.
dgn-np:NP394302.RA4qtaXGSU6-Wzx-jx47bMKxPPi3BrARxnn-ybwdYXcV8130_provenance
a
np:Provenance
.
dgn-np:NP394302.RA4qtaXGSU6-Wzx-jx47bMKxPPi3BrARxnn-ybwdYXcV8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP394302.RA4qtaXGSU6-Wzx-jx47bMKxPPi3BrARxnn-ybwdYXcV8130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0023787
a
ncit:C7057
.
dgn-gda:DGN2bbcba5e9e84b722064286268d4243a8
sio:SIO_000628
miriam-gene:4000
,
lld:C0023787
;
a
sio:SIO_001121
.
}
dgn-np:NP394302.RA4qtaXGSU6-Wzx-jx47bMKxPPi3BrARxnn-ybwdYXcV8130_provenance
{
dgn-np:NP394302.RA4qtaXGSU6-Wzx-jx47bMKxPPi3BrARxnn-ybwdYXcV8130_assertion
dcterms:description
"[For instance, evaluation of the clinical features of carriers of mutant LMNA in kindreds with familial partial lipodystrophy suggests rational, staged intervention using established pharmaceutical agents to prevent cardiovascular complications not just for patients with lipodystrophy but by extension for patients with the common metabolic syndrome.]. 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:17466974
;
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:NP394302.RA4qtaXGSU6-Wzx-jx47bMKxPPi3BrARxnn-ybwdYXcV8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:54+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" .
}