@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP411124.RA5_H8cEeeeU_ocx2t0gNehuiVuqwTUPF7uMJKAdAONIw
> .
@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:NP411124.RA5_H8cEeeeU_ocx2t0gNehuiVuqwTUPF7uMJKAdAONIw130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP411124.RA5_H8cEeeeU_ocx2t0gNehuiVuqwTUPF7uMJKAdAONIw130_publicationInfo
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a
np:Nanopublication
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a
np:Assertion
.
dgn-np:NP411124.RA5_H8cEeeeU_ocx2t0gNehuiVuqwTUPF7uMJKAdAONIw130_provenance
a
np:Provenance
.
dgn-np:NP411124.RA5_H8cEeeeU_ocx2t0gNehuiVuqwTUPF7uMJKAdAONIw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP411124.RA5_H8cEeeeU_ocx2t0gNehuiVuqwTUPF7uMJKAdAONIw130_assertion
{
miriam-gene:3627
a
ncit:C16612
.
lld:C0019163
a
ncit:C7057
.
dgn-gda:DGN1755014f9f796d440c04de7dd81ebe4c
sio:SIO_000628
miriam-gene:3627
,
lld:C0019163
;
a
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.
}
dgn-np:NP411124.RA5_H8cEeeeU_ocx2t0gNehuiVuqwTUPF7uMJKAdAONIw130_provenance
{
dgn-np:NP411124.RA5_H8cEeeeU_ocx2t0gNehuiVuqwTUPF7uMJKAdAONIw130_assertion
dcterms:description
"[We systematically screened sequence variations in the CXCL10 gene and examined the association between the variations in this gene and susceptibility to disease progression of chronic HBV infection in Chinese populations from Beijing and Chongqing.]. 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:18325387
;
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:NP411124.RA5_H8cEeeeU_ocx2t0gNehuiVuqwTUPF7uMJKAdAONIw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:04+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
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pav:authoredBy
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
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> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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