@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP189789.RAU5ypdvk0ZhE-IZk57nxp8RViZ8Mmf9ARVlVXbEGVpwk
> .
@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:NP189789.RAU5ypdvk0ZhE-IZk57nxp8RViZ8Mmf9ARVlVXbEGVpwk130_head
{
this:
np:hasAssertion
dgn-np:NP189789.RAU5ypdvk0ZhE-IZk57nxp8RViZ8Mmf9ARVlVXbEGVpwk130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP189789.RAU5ypdvk0ZhE-IZk57nxp8RViZ8Mmf9ARVlVXbEGVpwk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP189789.RAU5ypdvk0ZhE-IZk57nxp8RViZ8Mmf9ARVlVXbEGVpwk130_assertion
a
np:Assertion
.
dgn-np:NP189789.RAU5ypdvk0ZhE-IZk57nxp8RViZ8Mmf9ARVlVXbEGVpwk130_provenance
a
np:Provenance
.
dgn-np:NP189789.RAU5ypdvk0ZhE-IZk57nxp8RViZ8Mmf9ARVlVXbEGVpwk130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:55603
a
ncit:C16612
.
lld:C1956346
a
ncit:C7057
.
dgn-gda:DGN490bda9f6fe87090b0769758b9a9d947
sio:SIO_000628
miriam-gene:55603
,
lld:C1956346
;
a
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.
}
dgn-np:NP189789.RAU5ypdvk0ZhE-IZk57nxp8RViZ8Mmf9ARVlVXbEGVpwk130_provenance
{
dgn-np:NP189789.RAU5ypdvk0ZhE-IZk57nxp8RViZ8Mmf9ARVlVXbEGVpwk130_assertion
dcterms:description
"[The use of data on genetic variants and the addition of data on global monocytic gene expression led to the identification of the novel functional CAD susceptibility locus LIPA, located on chromosome 10q23.31. The respective eSNPs associated with CAD stro]. 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:21606135
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP189789.RAU5ypdvk0ZhE-IZk57nxp8RViZ8Mmf9ARVlVXbEGVpwk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:13+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
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;
pav:authoredBy
<
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> , <
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> , <
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
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pav:version
"v4.0.0" .
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