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http://rdf.disgenet.org/nanopublications.trig#NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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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#
> .
@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:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_assertion
;
np:hasProvenance
dgn-np:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_provenance
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np:hasPublicationInfo
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a
np:Nanopublication
.
dgn-np:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_assertion
a
np:Assertion
.
dgn-np:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_provenance
a
np:Provenance
.
dgn-np:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_publicationInfo
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{
miriam-gene:7305
a
ncit:C16612
.
lld:C0011303
a
ncit:C7057
.
dgn-gda:DGN75e90cfe141ee84aef250b6dbbab8d16
sio:SIO_000628
miriam-gene:7305
,
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;
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.
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dgn-np:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_provenance
{
dgn-np:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_assertion
dcterms:description
"[The genes of the DAP12-TREM2 signaling receptor are located on 19q13.12 and 6p21.1, to which linkage has been observed also in families affected by another immune-mediated demyelinating disease, MS. We have tested if allelic variation in DAP12 or TREM2 predisposes also to MS by monitoring carrier frequency of the Finnish PLOSL mutation in Finnish MS cases and by studying DAP12 and TREM2 in MS by linkage and association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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miriam-pubmed:19019460
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prov:wasGeneratedBy
eco:ECO_0000203
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dgn-void:befree-20140225
pav:importedOn
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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:NP345468.RAgDpooP_1cfVatwie86-aBSbOQSb1Pej9plE3Ksucno0130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
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> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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prv:usedData
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