@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP760308.RAYbBkhz_uvdmVqh7OqmkBBrHxbSE_w2vvZ6tUpLaO_FU
> .
@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#
> .
dgn-np:NP760308.RAYbBkhz_uvdmVqh7OqmkBBrHxbSE_w2vvZ6tUpLaO_FU130_head
{
this:
np:hasAssertion
dgn-np:NP760308.RAYbBkhz_uvdmVqh7OqmkBBrHxbSE_w2vvZ6tUpLaO_FU130_assertion
;
np:hasProvenance
dgn-np:NP760308.RAYbBkhz_uvdmVqh7OqmkBBrHxbSE_w2vvZ6tUpLaO_FU130_provenance
;
np:hasPublicationInfo
dgn-np:NP760308.RAYbBkhz_uvdmVqh7OqmkBBrHxbSE_w2vvZ6tUpLaO_FU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP760308.RAYbBkhz_uvdmVqh7OqmkBBrHxbSE_w2vvZ6tUpLaO_FU130_assertion
a
np:Assertion
.
dgn-np:NP760308.RAYbBkhz_uvdmVqh7OqmkBBrHxbSE_w2vvZ6tUpLaO_FU130_provenance
a
np:Provenance
.
dgn-np:NP760308.RAYbBkhz_uvdmVqh7OqmkBBrHxbSE_w2vvZ6tUpLaO_FU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP760308.RAYbBkhz_uvdmVqh7OqmkBBrHxbSE_w2vvZ6tUpLaO_FU130_assertion
{
miriam-gene:7099
a
ncit:C16612
.
lld:C0262655
a
ncit:C7057
.
dgn-gda:DGN5d7a0a0f9a4552517c3d934f536a852e
sio:SIO_000628
miriam-gene:7099
,
lld:C0262655
;
a
sio:SIO_001121
.
}
dgn-np:NP760308.RAYbBkhz_uvdmVqh7OqmkBBrHxbSE_w2vvZ6tUpLaO_FU130_provenance
{
dgn-np:NP760308.RAYbBkhz_uvdmVqh7OqmkBBrHxbSE_w2vvZ6tUpLaO_FU130_assertion
dcterms:description
"[Our data indicates a relationship between the carrier status of HSPA1B (1267)G and TLR4 (896)G alleles and the development of recurrent UTI in childhood independently of other renal abnormalities, while raising further questions about the clinical and therapeutic relevance of these polymorphisms in everyday pediatric nephrology.]. 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:17314700
;
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 .
}
dgn-np:NP760308.RAYbBkhz_uvdmVqh7OqmkBBrHxbSE_w2vvZ6tUpLaO_FU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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
"v2.1.0.0" .
dgn-void:disgenetrdf
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"v2.1.0" .
}