@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP608288.RAoL3jU5nmiWaokS_LAF1oeVLq51OC97nYxT9ntoaPUqY
> .
@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:NP608288.RAoL3jU5nmiWaokS_LAF1oeVLq51OC97nYxT9ntoaPUqY130_head
{
this:
np:hasAssertion
dgn-np:NP608288.RAoL3jU5nmiWaokS_LAF1oeVLq51OC97nYxT9ntoaPUqY130_assertion
;
np:hasProvenance
dgn-np:NP608288.RAoL3jU5nmiWaokS_LAF1oeVLq51OC97nYxT9ntoaPUqY130_provenance
;
np:hasPublicationInfo
dgn-np:NP608288.RAoL3jU5nmiWaokS_LAF1oeVLq51OC97nYxT9ntoaPUqY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP608288.RAoL3jU5nmiWaokS_LAF1oeVLq51OC97nYxT9ntoaPUqY130_assertion
a
np:Assertion
.
dgn-np:NP608288.RAoL3jU5nmiWaokS_LAF1oeVLq51OC97nYxT9ntoaPUqY130_provenance
a
np:Provenance
.
dgn-np:NP608288.RAoL3jU5nmiWaokS_LAF1oeVLq51OC97nYxT9ntoaPUqY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP608288.RAoL3jU5nmiWaokS_LAF1oeVLq51OC97nYxT9ntoaPUqY130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0019693
a
ncit:C7057
.
dgn-gda:DGNf562ae334bbbefdde508d6705394f28f
sio:SIO_000628
miriam-gene:3126
,
lld:C0019693
;
a
sio:SIO_001121
.
}
dgn-np:NP608288.RAoL3jU5nmiWaokS_LAF1oeVLq51OC97nYxT9ntoaPUqY130_provenance
{
dgn-np:NP608288.RAoL3jU5nmiWaokS_LAF1oeVLq51OC97nYxT9ntoaPUqY130_assertion
dcterms:description
"[Genetic variation at the human leukocyte antigen (HLA) loci has been shown to be an important risk factor for progression to HIV disease, but its significance in infection is less well understood.]. 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:11464148
;
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:NP608288.RAoL3jU5nmiWaokS_LAF1oeVLq51OC97nYxT9ntoaPUqY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:05+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" .
}