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http://rdf.disgenet.org/nanopublications.trig#NP768704.RA5_0BM6R1NNFqDVFIYn2sqh1W3JNsnkkJp1VRFFDLfZc
> .
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> .
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http://www.w3.org/2001/XMLSchema#
> .
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http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP768704.RA5_0BM6R1NNFqDVFIYn2sqh1W3JNsnkkJp1VRFFDLfZc130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP768704.RA5_0BM6R1NNFqDVFIYn2sqh1W3JNsnkkJp1VRFFDLfZc130_publicationInfo
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP768704.RA5_0BM6R1NNFqDVFIYn2sqh1W3JNsnkkJp1VRFFDLfZc130_provenance
a
np:Provenance
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dgn-np:NP768704.RA5_0BM6R1NNFqDVFIYn2sqh1W3JNsnkkJp1VRFFDLfZc130_publicationInfo
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{
miriam-gene:4023
a
ncit:C16612
.
lld:C0007785
a
ncit:C7057
.
dgn-gda:DGN5ed91e1d8475e7c3ad34b70256f66d48
sio:SIO_000628
miriam-gene:4023
,
lld:C0007785
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.
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dgn-np:NP768704.RA5_0BM6R1NNFqDVFIYn2sqh1W3JNsnkkJp1VRFFDLfZc130_provenance
{
dgn-np:NP768704.RA5_0BM6R1NNFqDVFIYn2sqh1W3JNsnkkJp1VRFFDLfZc130_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
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prov:wasGeneratedBy
eco:ECO_0000203
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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:NP768704.RA5_0BM6R1NNFqDVFIYn2sqh1W3JNsnkkJp1VRFFDLfZc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:45+02:00"^^
xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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<
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> , <
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> , <
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> , <
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> ;
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<
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