@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP61133.RA1S1IBSGkQQfY5rZxv8s-X9mGLX9At8z20AMZGbdAhuc
> .
@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:NP61133.RA1S1IBSGkQQfY5rZxv8s-X9mGLX9At8z20AMZGbdAhuc130_head
{
this:
np:hasAssertion
dgn-np:NP61133.RA1S1IBSGkQQfY5rZxv8s-X9mGLX9At8z20AMZGbdAhuc130_assertion
;
np:hasProvenance
dgn-np:NP61133.RA1S1IBSGkQQfY5rZxv8s-X9mGLX9At8z20AMZGbdAhuc130_provenance
;
np:hasPublicationInfo
dgn-np:NP61133.RA1S1IBSGkQQfY5rZxv8s-X9mGLX9At8z20AMZGbdAhuc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP61133.RA1S1IBSGkQQfY5rZxv8s-X9mGLX9At8z20AMZGbdAhuc130_assertion
a
np:Assertion
.
dgn-np:NP61133.RA1S1IBSGkQQfY5rZxv8s-X9mGLX9At8z20AMZGbdAhuc130_provenance
a
np:Provenance
.
dgn-np:NP61133.RA1S1IBSGkQQfY5rZxv8s-X9mGLX9At8z20AMZGbdAhuc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP61133.RA1S1IBSGkQQfY5rZxv8s-X9mGLX9At8z20AMZGbdAhuc130_assertion
{
miriam-gene:3812
a
ncit:C16612
.
lld:C0302592
a
ncit:C7057
.
dgn-gda:DGN29dccd3b2ba13ab657a02e19215f92ba
sio:SIO_000628
miriam-gene:3812
,
lld:C0302592
;
a
sio:SIO_001122
.
}
dgn-np:NP61133.RA1S1IBSGkQQfY5rZxv8s-X9mGLX9At8z20AMZGbdAhuc130_provenance
{
dgn-np:NP61133.RA1S1IBSGkQQfY5rZxv8s-X9mGLX9At8z20AMZGbdAhuc130_assertion
dcterms:description
"[The system has been applied to a healthy Northern Irish control group, establishing frequencies for this Caucasian population. Additionally, the KIR3DL2 allele status of cell line DNA and Centre d'Etude du Polymorphisme Humain (CEPH) families, both from the 13th International Histocompatibility Workshop, has been established. A high level of KIR3DL2 allelic polymorphism has been identified.]. 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:15304002
;
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:NP61133.RA1S1IBSGkQQfY5rZxv8s-X9mGLX9At8z20AMZGbdAhuc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}