@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP399262.RAYIHSW3nJscPJaEJdxgar7BHN0YxzrdqL6Q3r9yfowTA
> .
@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:NP399262.RAYIHSW3nJscPJaEJdxgar7BHN0YxzrdqL6Q3r9yfowTA130_head
{
this:
np:hasAssertion
dgn-np:NP399262.RAYIHSW3nJscPJaEJdxgar7BHN0YxzrdqL6Q3r9yfowTA130_assertion
;
np:hasProvenance
dgn-np:NP399262.RAYIHSW3nJscPJaEJdxgar7BHN0YxzrdqL6Q3r9yfowTA130_provenance
;
np:hasPublicationInfo
dgn-np:NP399262.RAYIHSW3nJscPJaEJdxgar7BHN0YxzrdqL6Q3r9yfowTA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP399262.RAYIHSW3nJscPJaEJdxgar7BHN0YxzrdqL6Q3r9yfowTA130_assertion
a
np:Assertion
.
dgn-np:NP399262.RAYIHSW3nJscPJaEJdxgar7BHN0YxzrdqL6Q3r9yfowTA130_provenance
a
np:Provenance
.
dgn-np:NP399262.RAYIHSW3nJscPJaEJdxgar7BHN0YxzrdqL6Q3r9yfowTA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP399262.RAYIHSW3nJscPJaEJdxgar7BHN0YxzrdqL6Q3r9yfowTA130_assertion
{
miriam-gene:3988
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN8a952d6a191c9a1982a223186eeafd84
sio:SIO_000628
miriam-gene:3988
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP399262.RAYIHSW3nJscPJaEJdxgar7BHN0YxzrdqL6Q3r9yfowTA130_provenance
{
dgn-np:NP399262.RAYIHSW3nJscPJaEJdxgar7BHN0YxzrdqL6Q3r9yfowTA130_assertion
dcterms:description
"[Four gene variants related to lipid metabolism (including the rs562338 and rs503662 variants of the APOB gene, the rs7767084 variant of the LPA gene and the rs2246942 variant of the LIPA gene) have been shown to be associated with coronary heart disease (CHD).]. 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:23653095
;
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:NP399262.RAYIHSW3nJscPJaEJdxgar7BHN0YxzrdqL6Q3r9yfowTA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:58+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" .
}