@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP681750.RADXAb7WlYUN_F9HJQAp9ADBixDQwSY0mEoiqBBc0gww0
> .
@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:NP681750.RADXAb7WlYUN_F9HJQAp9ADBixDQwSY0mEoiqBBc0gww0130_head
{
this:
np:hasAssertion
dgn-np:NP681750.RADXAb7WlYUN_F9HJQAp9ADBixDQwSY0mEoiqBBc0gww0130_assertion
;
np:hasProvenance
dgn-np:NP681750.RADXAb7WlYUN_F9HJQAp9ADBixDQwSY0mEoiqBBc0gww0130_provenance
;
np:hasPublicationInfo
dgn-np:NP681750.RADXAb7WlYUN_F9HJQAp9ADBixDQwSY0mEoiqBBc0gww0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP681750.RADXAb7WlYUN_F9HJQAp9ADBixDQwSY0mEoiqBBc0gww0130_assertion
a
np:Assertion
.
dgn-np:NP681750.RADXAb7WlYUN_F9HJQAp9ADBixDQwSY0mEoiqBBc0gww0130_provenance
a
np:Provenance
.
dgn-np:NP681750.RADXAb7WlYUN_F9HJQAp9ADBixDQwSY0mEoiqBBc0gww0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP681750.RADXAb7WlYUN_F9HJQAp9ADBixDQwSY0mEoiqBBc0gww0130_assertion
{
miriam-gene:3565
a
ncit:C16612
.
lld:C0027726
a
ncit:C7057
.
dgn-gda:DGNcd6669fb057056354a1d964be54b0ac0
sio:SIO_000628
miriam-gene:3565
,
lld:C0027726
;
a
sio:SIO_001121
.
}
dgn-np:NP681750.RADXAb7WlYUN_F9HJQAp9ADBixDQwSY0mEoiqBBc0gww0130_provenance
{
dgn-np:NP681750.RADXAb7WlYUN_F9HJQAp9ADBixDQwSY0mEoiqBBc0gww0130_assertion
dcterms:description
"[We conclude that polymorphisms in the IL4 receptor, the high-affinity IgE receptor and IL13 do not seem to predict the clinical course of NS, despite the fact that serum IgE elevations are more frequent in patients with NS than in normal control subjects.]. 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:11980568
;
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:NP681750.RADXAb7WlYUN_F9HJQAp9ADBixDQwSY0mEoiqBBc0gww0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:51+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" .
}