@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0
> .
@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
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_publicationInfo
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a
np:Nanopublication
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a
np:Assertion
.
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a
np:Provenance
.
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a
np:PublicationInfo
.
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dgn-np:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_assertion
{
miriam-gene:11330
a
ncit:C16612
.
lld:C0149521
a
ncit:C7057
.
dgn-gda:DGNda755bae6f96ccf81a4a740c64c4a169
sio:SIO_000628
miriam-gene:11330
,
lld:C0149521
;
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.
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dgn-np:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_provenance
{
dgn-np:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_assertion
dcterms:description
"[The authors sequenced all eight exons and flanking regions in CTRC in 584 CP patients (497 TCP, 87 idiopathic CP) and 598 normal subjects and analysed the significance of association using χ(2) test.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:22580415
;
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:NP490448.RA3XriH508NOfMMOt2iJQW4tBprUTeeIGEnio9x4uw3e0130_publicationInfo
{
this:
dcterms:created
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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
;
prv:usedData
dgn-void:disgenetrdf
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<
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> , <
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> , <
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> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
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pav:version
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