@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP50843.RA7gT5gEwgSCzh2maYFkpIzpD0dG7h-4mQraAGiv9IGbg
> .
@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:NP50843.RA7gT5gEwgSCzh2maYFkpIzpD0dG7h-4mQraAGiv9IGbg130_head
{
this:
np:hasAssertion
dgn-np:NP50843.RA7gT5gEwgSCzh2maYFkpIzpD0dG7h-4mQraAGiv9IGbg130_assertion
;
np:hasProvenance
dgn-np:NP50843.RA7gT5gEwgSCzh2maYFkpIzpD0dG7h-4mQraAGiv9IGbg130_provenance
;
np:hasPublicationInfo
dgn-np:NP50843.RA7gT5gEwgSCzh2maYFkpIzpD0dG7h-4mQraAGiv9IGbg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP50843.RA7gT5gEwgSCzh2maYFkpIzpD0dG7h-4mQraAGiv9IGbg130_assertion
a
np:Assertion
.
dgn-np:NP50843.RA7gT5gEwgSCzh2maYFkpIzpD0dG7h-4mQraAGiv9IGbg130_provenance
a
np:Provenance
.
dgn-np:NP50843.RA7gT5gEwgSCzh2maYFkpIzpD0dG7h-4mQraAGiv9IGbg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP50843.RA7gT5gEwgSCzh2maYFkpIzpD0dG7h-4mQraAGiv9IGbg130_assertion
{
miriam-gene:6891
a
ncit:C16612
.
lld:C0553662
a
ncit:C7057
.
dgn-gda:DGN16a205dde714ffdafa994441661b967d
sio:SIO_000628
miriam-gene:6891
,
lld:C0553662
;
a
sio:SIO_001122
.
}
dgn-np:NP50843.RA7gT5gEwgSCzh2maYFkpIzpD0dG7h-4mQraAGiv9IGbg130_provenance
{
dgn-np:NP50843.RA7gT5gEwgSCzh2maYFkpIzpD0dG7h-4mQraAGiv9IGbg130_assertion
dcterms:description
"[Such complexity of TAP2 polymorphisms, in the form of SNPs as well as alleles, is likely to complicate the analyses of disease associations and haplotype structures in the HLA class II region.]. 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:11294565
;
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:NP50843.RA7gT5gEwgSCzh2maYFkpIzpD0dG7h-4mQraAGiv9IGbg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:23+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" .
}