@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4
> .
@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:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_head
{
this:
np:hasAssertion
dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_assertion
;
np:hasProvenance
dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_provenance
;
np:hasPublicationInfo
dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_assertion
a
np:Assertion
.
dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_provenance
a
np:Provenance
.
dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_assertion
{
miriam-gene:79068
a
ncit:C16612
.
lld:C0524620
a
ncit:C7057
.
dgn-gda:DGN47eff6c2fc1fd20c34e3752b9df04549
sio:SIO_000628
miriam-gene:79068
,
lld:C0524620
;
a
sio:SIO_001122
.
}
dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_provenance
{
dgn-np:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_assertion
dcterms:description
"[Our findings suggest that genes from lipid metabolism pathways have the key role in the genetic background of MetS. We found little evidence for pleiotropy linking dyslipidemia and obesity to the other MetS component traits, such as hypertension and glucose intolerance.]. 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:22399527
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP71766.RAxmQQUfCWdTvMwMLSZPUFldHksHLpwj8BVk6f6qhJCt4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:35+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" .
}