@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570
> .
@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:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_head
{
this:
np:hasAssertion
dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_assertion
;
np:hasProvenance
dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_provenance
;
np:hasPublicationInfo
dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_assertion
a
np:Assertion
.
dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_provenance
a
np:Provenance
.
dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_assertion
{
miriam-gene:3566
a
ncit:C16612
.
lld:C0026769
a
ncit:C7057
.
dgn-gda:DGNd475ec0a292376c81af3a45e95ffdcaf
sio:SIO_000628
miriam-gene:3566
,
lld:C0026769
;
a
sio:SIO_001121
.
}
dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_provenance
{
dgn-np:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_assertion
dcterms:description
"[By genotyping two promoter and eight coding IL4R SNPs and identifying haplotypes (complex alleles) in the MS families, stratified for HLA genotype, we have observed evidence of the association of the IL4R gene to MS.]. 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:14712310
;
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:NP440356.RAPlrn1tlrgdVqPLwoB6CCSyNRfiGnTVnP1BG-iSsn570130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
}