@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU
> .
@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 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:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_head
{
this:
np:hasAssertion
dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_assertion
;
np:hasProvenance
dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_provenance
;
np:hasPublicationInfo
dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_assertion
a
np:Assertion
.
dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_provenance
a
np:Provenance
.
dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_assertion
{
miriam-gene:80352
a
ncit:C16612
.
lld:C0019693
a
ncit:C7057
.
dgn-gda:DGN8ae3092ec1f184a3a4e68071430244de
sio:SIO_000628
miriam-gene:80352
,
lld:C0019693
;
a
sio:SIO_001122
.
}
dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_provenance
{
dgn-np:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_assertion
dct:description
"[A genome-wide association study of people with incident human immunodeficiency virus (HIV) infection selected from nine different cohorts identified allelic polymorphisms, which associated with either viral set point (HCP5 and 5' HLA-C) or with HIV disease progression (RNF39 and ZNRD1).]. 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:19693088
;
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:NP78161.RA4TedKzq-bLQzcOnjKGdW6FitXK03fs6Nkww8A0TBMtU130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:38+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}