@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP86632.RA3TIuDQiHPe7cNdOkG3RdqCj3tri8OU9WTcGLAdRydcE
> .
@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:NP86632.RA3TIuDQiHPe7cNdOkG3RdqCj3tri8OU9WTcGLAdRydcE130_head
{
this:
np:hasAssertion
dgn-np:NP86632.RA3TIuDQiHPe7cNdOkG3RdqCj3tri8OU9WTcGLAdRydcE130_assertion
;
np:hasProvenance
dgn-np:NP86632.RA3TIuDQiHPe7cNdOkG3RdqCj3tri8OU9WTcGLAdRydcE130_provenance
;
np:hasPublicationInfo
dgn-np:NP86632.RA3TIuDQiHPe7cNdOkG3RdqCj3tri8OU9WTcGLAdRydcE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP86632.RA3TIuDQiHPe7cNdOkG3RdqCj3tri8OU9WTcGLAdRydcE130_assertion
a
np:Assertion
.
dgn-np:NP86632.RA3TIuDQiHPe7cNdOkG3RdqCj3tri8OU9WTcGLAdRydcE130_provenance
a
np:Provenance
.
dgn-np:NP86632.RA3TIuDQiHPe7cNdOkG3RdqCj3tri8OU9WTcGLAdRydcE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP86632.RA3TIuDQiHPe7cNdOkG3RdqCj3tri8OU9WTcGLAdRydcE130_assertion
{
miriam-gene:3552
a
ncit:C16612
.
lld:C0002986
a
ncit:C7057
.
dgn-gda:DGN5ecdb4cc2edc375f6e7cb82068833dbb
sio:SIO_000628
miriam-gene:3552
,
lld:C0002986
;
a
sio:SIO_001122
.
}
dgn-np:NP86632.RA3TIuDQiHPe7cNdOkG3RdqCj3tri8OU9WTcGLAdRydcE130_provenance
{
dgn-np:NP86632.RA3TIuDQiHPe7cNdOkG3RdqCj3tri8OU9WTcGLAdRydcE130_assertion
dcterms:description
"[We speculate that sequence variations of important inflammatory genes of the interleukin inflammatory family are associated with differential effects in Fabry disease, and with increased sample size, haplotype blocks might be constructed.]. 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:17353161
;
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 .
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dgn-np:NP86632.RA3TIuDQiHPe7cNdOkG3RdqCj3tri8OU9WTcGLAdRydcE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:42+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" .
}