@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP70368.RAszsYAYRvKsev0jjjwaj0JX3zrmPUXRFsnsNnUWNrOnA
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP70368.RAszsYAYRvKsev0jjjwaj0JX3zrmPUXRFsnsNnUWNrOnA130_head
{
this:
np:hasAssertion
dgn-np:NP70368.RAszsYAYRvKsev0jjjwaj0JX3zrmPUXRFsnsNnUWNrOnA130_assertion
;
np:hasProvenance
dgn-np:NP70368.RAszsYAYRvKsev0jjjwaj0JX3zrmPUXRFsnsNnUWNrOnA130_provenance
;
np:hasPublicationInfo
dgn-np:NP70368.RAszsYAYRvKsev0jjjwaj0JX3zrmPUXRFsnsNnUWNrOnA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP70368.RAszsYAYRvKsev0jjjwaj0JX3zrmPUXRFsnsNnUWNrOnA130_assertion
a
np:Assertion
.
dgn-np:NP70368.RAszsYAYRvKsev0jjjwaj0JX3zrmPUXRFsnsNnUWNrOnA130_provenance
a
np:Provenance
.
dgn-np:NP70368.RAszsYAYRvKsev0jjjwaj0JX3zrmPUXRFsnsNnUWNrOnA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP70368.RAszsYAYRvKsev0jjjwaj0JX3zrmPUXRFsnsNnUWNrOnA130_assertion
{
miriam-gene:3690
a
ncit:C16612
.
lld:C0024314
a
ncit:C7057
.
dgn-gda:DGNc53edbb92c3256f9debf664c51184165
sio:SIO_000628
miriam-gene:3690
,
lld:C0024314
;
a
sio:SIO_001122
.
}
dgn-np:NP70368.RAszsYAYRvKsev0jjjwaj0JX3zrmPUXRFsnsNnUWNrOnA130_provenance
{
dgn-np:NP70368.RAszsYAYRvKsev0jjjwaj0JX3zrmPUXRFsnsNnUWNrOnA130_assertion
dcterms:description
"[This study is of great importance (i) particularly in the context of the diversity caused by the population migrations, we may observe today in our hospitals (ii) to confirm that the Pygmy population with distinctive frequencies (absence of the HPA-1b, HP]. 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:15730528
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP70368.RAszsYAYRvKsev0jjjwaj0JX3zrmPUXRFsnsNnUWNrOnA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:38:18+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}