@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP304626.RA0kT1xBIhOHZrv7ShZdBps9KacV0uJI0COL_u5-pJKbs
> .
@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:NP304626.RA0kT1xBIhOHZrv7ShZdBps9KacV0uJI0COL_u5-pJKbs130_head
{
this:
np:hasAssertion
dgn-np:NP304626.RA0kT1xBIhOHZrv7ShZdBps9KacV0uJI0COL_u5-pJKbs130_assertion
;
np:hasProvenance
dgn-np:NP304626.RA0kT1xBIhOHZrv7ShZdBps9KacV0uJI0COL_u5-pJKbs130_provenance
;
np:hasPublicationInfo
dgn-np:NP304626.RA0kT1xBIhOHZrv7ShZdBps9KacV0uJI0COL_u5-pJKbs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP304626.RA0kT1xBIhOHZrv7ShZdBps9KacV0uJI0COL_u5-pJKbs130_assertion
a
np:Assertion
.
dgn-np:NP304626.RA0kT1xBIhOHZrv7ShZdBps9KacV0uJI0COL_u5-pJKbs130_provenance
a
np:Provenance
.
dgn-np:NP304626.RA0kT1xBIhOHZrv7ShZdBps9KacV0uJI0COL_u5-pJKbs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP304626.RA0kT1xBIhOHZrv7ShZdBps9KacV0uJI0COL_u5-pJKbs130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0524620
a
ncit:C7057
.
dgn-gda:DGN35848b4a11dfc85703012fc8fae41441
sio:SIO_000628
miriam-gene:4000
,
lld:C0524620
;
a
sio:SIO_001121
.
}
dgn-np:NP304626.RA0kT1xBIhOHZrv7ShZdBps9KacV0uJI0COL_u5-pJKbs130_provenance
{
dgn-np:NP304626.RA0kT1xBIhOHZrv7ShZdBps9KacV0uJI0COL_u5-pJKbs130_assertion
dcterms:description
"[In 971 participants from the Amish Family Diabetes Study, the H566H polymorphism of LMNA was associated with metabolic syndrome diagnosed according to National Cholesterol Education Program ATP III criteria and also higher mean fasting triglyceride and lower mean high-density lipoprotein-cholesterol concentrations.]. 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:15205219
;
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:NP304626.RA0kT1xBIhOHZrv7ShZdBps9KacV0uJI0COL_u5-pJKbs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:55+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" .
}