@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP181833.RATJRY3x8BlTedy3bUSK8xyYNzVqxCIn5lMvDMjKjf-kI
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP181833.RATJRY3x8BlTedy3bUSK8xyYNzVqxCIn5lMvDMjKjf-kI130_assertion
;
np:hasProvenance
dgn-np:NP181833.RATJRY3x8BlTedy3bUSK8xyYNzVqxCIn5lMvDMjKjf-kI130_provenance
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np:hasPublicationInfo
dgn-np:NP181833.RATJRY3x8BlTedy3bUSK8xyYNzVqxCIn5lMvDMjKjf-kI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP181833.RATJRY3x8BlTedy3bUSK8xyYNzVqxCIn5lMvDMjKjf-kI130_assertion
a
np:Assertion
.
dgn-np:NP181833.RATJRY3x8BlTedy3bUSK8xyYNzVqxCIn5lMvDMjKjf-kI130_provenance
a
np:Provenance
.
dgn-np:NP181833.RATJRY3x8BlTedy3bUSK8xyYNzVqxCIn5lMvDMjKjf-kI130_publicationInfo
a
np:PublicationInfo
.
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dgn-np:NP181833.RATJRY3x8BlTedy3bUSK8xyYNzVqxCIn5lMvDMjKjf-kI130_assertion
{
miriam-gene:4023
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGN402bfef308bb4ffa9393a0f502c297bb
sio:SIO_000628
miriam-gene:4023
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP181833.RATJRY3x8BlTedy3bUSK8xyYNzVqxCIn5lMvDMjKjf-kI130_provenance
{
dgn-np:NP181833.RATJRY3x8BlTedy3bUSK8xyYNzVqxCIn5lMvDMjKjf-kI130_assertion
dcterms:description
"[We first studied the relationship between LPL polymorphisms and the risk of atherosclerotic cerebral infarction (CI) by detecting the frequencies of LPL HindIII, PvuII and Ser447Ter genotypes and combined genotypes in the Chinese.]. 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:18590804
;
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 .
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dgn-np:NP181833.RATJRY3x8BlTedy3bUSK8xyYNzVqxCIn5lMvDMjKjf-kI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:38+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
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dgn-void:disgenetrdf
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}