@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP403772.RAcJl3c0i92-UAuTODSvApkQwBclILSOWQhOceZlorQ3c
> .
@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:NP403772.RAcJl3c0i92-UAuTODSvApkQwBclILSOWQhOceZlorQ3c130_head
{
this:
np:hasAssertion
dgn-np:NP403772.RAcJl3c0i92-UAuTODSvApkQwBclILSOWQhOceZlorQ3c130_assertion
;
np:hasProvenance
dgn-np:NP403772.RAcJl3c0i92-UAuTODSvApkQwBclILSOWQhOceZlorQ3c130_provenance
;
np:hasPublicationInfo
dgn-np:NP403772.RAcJl3c0i92-UAuTODSvApkQwBclILSOWQhOceZlorQ3c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP403772.RAcJl3c0i92-UAuTODSvApkQwBclILSOWQhOceZlorQ3c130_assertion
a
np:Assertion
.
dgn-np:NP403772.RAcJl3c0i92-UAuTODSvApkQwBclILSOWQhOceZlorQ3c130_provenance
a
np:Provenance
.
dgn-np:NP403772.RAcJl3c0i92-UAuTODSvApkQwBclILSOWQhOceZlorQ3c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP403772.RAcJl3c0i92-UAuTODSvApkQwBclILSOWQhOceZlorQ3c130_assertion
{
miriam-gene:3126
a
ncit:C16612
.
lld:C0042769
a
ncit:C7057
.
dgn-gda:DGNe7f361f3831dd8f7148c3d807d1f368b
sio:SIO_000628
miriam-gene:3126
,
lld:C0042769
;
a
sio:SIO_001121
.
}
dgn-np:NP403772.RAcJl3c0i92-UAuTODSvApkQwBclILSOWQhOceZlorQ3c130_provenance
{
dgn-np:NP403772.RAcJl3c0i92-UAuTODSvApkQwBclILSOWQhOceZlorQ3c130_assertion
dcterms:description
"[Considering HLA polymorphism in terms of supertype diversity is recommended in strategies to design association studies for robust results across populations and in trials to improve treatment options for patients with chronic viral infection.]. 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:17935228
;
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:NP403772.RAcJl3c0i92-UAuTODSvApkQwBclILSOWQhOceZlorQ3c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:00+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" .
}