@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY
> .
@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:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_head
{
this:
np:hasAssertion
dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_assertion
;
np:hasProvenance
dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_provenance
;
np:hasPublicationInfo
dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_assertion
a
np:Assertion
.
dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_provenance
a
np:Provenance
.
dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_assertion
{
miriam-gene:4713
a
ncit:C16612
.
lld:C0011854
a
ncit:C7057
.
dgn-gda:DGN5a5a8f51a5562590837d217628c08b6a
sio:SIO_000628
miriam-gene:4713
,
lld:C0011854
;
a
sio:SIO_001121
.
}
dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_provenance
{
dgn-np:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_assertion
dcterms:description
"[The extended HLA haplotype B18 CF130 DR3 DQw2, which is common (around 10% phenotype frequency) in healthy Spaniards and in other populations of paleo-North African origin, was found to be significantly less frequent in NIDD, JRA and BD, whereas its frequency was normal in IDD (although DR3 DQw2 haplotypes were increased in the latter disease).]. 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:8335082
;
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:NP352803.RAEixkD7NRr6qspjOJyzP9vxZSPGhTIxKz-2MHV56nyIY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:27+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" .
}