@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54
> .
@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:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_head
{
this:
np:hasAssertion
dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_assertion
;
np:hasProvenance
dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_provenance
;
np:hasPublicationInfo
dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_assertion
a
np:Assertion
.
dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_provenance
a
np:Provenance
.
dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_assertion
{
miriam-gene:3586
a
ncit:C16612
.
lld:C0010346
a
ncit:C7057
.
dgn-gda:DGN5a13944dede48714d5d0f097813d737f
sio:SIO_000628
miriam-gene:3586
,
lld:C0010346
;
a
sio:SIO_001122
.
}
dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_provenance
{
dgn-np:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_assertion
dcterms:description
"[ Allele A of the Hsp70-2 gene may be associated with a less severe form of CD, suggesting the clinical value of the genotype assessment. The genetic determination of the defense mechanisms in CD appears to be associated with the polymorphism of the Hsp70-2 gene rather than that of the CD14 or IL-10 genes.]. 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:16165702
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP56718.RATtooZ08PvvOCqYqls2URm4aq-qIR_67jvT-p3d3sU54130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:26+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
pav:version
"v2.1.0" .
}