@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE
> .
@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:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_head
{
this:
np:hasAssertion
dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_assertion
;
np:hasProvenance
dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_provenance
;
np:hasPublicationInfo
dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_assertion
a
np:Assertion
.
dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_provenance
a
np:Provenance
.
dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_assertion
{
miriam-gene:1493
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN8f9b0f2fdf0603ff486d94576785bc02
sio:SIO_000628
miriam-gene:1493
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_provenance
{
dgn-np:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_assertion
dcterms:description
"[The observed decrease in the frequency of GG genotype in the breast cancer patients is contrary to the frequently reported increase of GG genotype in autoimmune diseases. In addition, the data implies that polymorphism of ctla-4 exon 1 contributes in tumor progression.]. 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:15218356
;
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:NP46474.RAdR-yUWipy2ELhNjlsv4dBiB4fXY1x3Ck3NeA48M5SHE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}