@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1141435.RA-vECHAGq840RohdQm4xfy3F-XOva5gt-YvDxNwRrK3c
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1141435.RA-vECHAGq840RohdQm4xfy3F-XOva5gt-YvDxNwRrK3c130_head
{
this:
np:hasAssertion
dgn-np:NP1141435.RA-vECHAGq840RohdQm4xfy3F-XOva5gt-YvDxNwRrK3c130_assertion
;
np:hasProvenance
dgn-np:NP1141435.RA-vECHAGq840RohdQm4xfy3F-XOva5gt-YvDxNwRrK3c130_provenance
;
np:hasPublicationInfo
dgn-np:NP1141435.RA-vECHAGq840RohdQm4xfy3F-XOva5gt-YvDxNwRrK3c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1141435.RA-vECHAGq840RohdQm4xfy3F-XOva5gt-YvDxNwRrK3c130_assertion
a
np:Assertion
.
dgn-np:NP1141435.RA-vECHAGq840RohdQm4xfy3F-XOva5gt-YvDxNwRrK3c130_provenance
a
np:Provenance
.
dgn-np:NP1141435.RA-vECHAGq840RohdQm4xfy3F-XOva5gt-YvDxNwRrK3c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1141435.RA-vECHAGq840RohdQm4xfy3F-XOva5gt-YvDxNwRrK3c130_assertion
{
miriam-gene:3358
a
ncit:C16612
.
lld:C0007222
a
ncit:C7057
.
dgn-gda:DGN74c3d0de8a46b4bfbff69f8ee6379b68
sio:SIO_000628
miriam-gene:3358
,
lld:C0007222
;
a
sio:SIO_001122
.
}
dgn-np:NP1141435.RA-vECHAGq840RohdQm4xfy3F-XOva5gt-YvDxNwRrK3c130_provenance
{
dgn-np:NP1141435.RA-vECHAGq840RohdQm4xfy3F-XOva5gt-YvDxNwRrK3c130_assertion
dcterms:description
"[These findings suggest that this functional polymorphism of the 5HTR2C gene is associated with increased risk for CVD mortality and morbidity, but this association is apparently not explained by the association of rs6318 with traditional risk factors or conventional markers of atherosclerotic disease.]. 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:24386118
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1141435.RA-vECHAGq840RohdQm4xfy3F-XOva5gt-YvDxNwRrK3c130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:23+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}