@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU
> .
@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:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_head
{
this:
np:hasAssertion
dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_assertion
;
np:hasProvenance
dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_provenance
;
np:hasPublicationInfo
dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_assertion
a
np:Assertion
.
dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_provenance
a
np:Provenance
.
dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_assertion
{
miriam-gene:1493
a
ncit:C16612
.
lld:C0042900
a
ncit:C7057
.
dgn-gda:DGN3e5c86685d9d78ecbfb7f90fed3fa545
sio:SIO_000628
miriam-gene:1493
,
lld:C0042900
;
a
sio:SIO_001121
.
}
dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_provenance
{
dgn-np:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_assertion
dcterms:description
"[CTLA-4 gene microsatellite polymorphisms were determined for 74 vitiligo patients (53 without any autoimmune disorder; 21 with one or more autoimmune disease) and 173 healthy controls, who had no clinical evidence of either vitiligo or any other autoimmune disorder, by polymerase chain reaction amplification of genomic DNA and resolution of the products on polyacrylamide sequencing gels.]. 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:10215771
;
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:NP843590.RA1kIxfxFET1nAeH-I_RcV1fP-vPKWMSXSkc_SFzXnHCU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:35+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" .
}