@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP934728.RA0ypCWf4wHof0VoEeDbenv4kC0sHeVe5QgUOR5YH0FPU
> .
@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:NP934728.RA0ypCWf4wHof0VoEeDbenv4kC0sHeVe5QgUOR5YH0FPU130_head
{
this:
np:hasAssertion
dgn-np:NP934728.RA0ypCWf4wHof0VoEeDbenv4kC0sHeVe5QgUOR5YH0FPU130_assertion
;
np:hasProvenance
dgn-np:NP934728.RA0ypCWf4wHof0VoEeDbenv4kC0sHeVe5QgUOR5YH0FPU130_provenance
;
np:hasPublicationInfo
dgn-np:NP934728.RA0ypCWf4wHof0VoEeDbenv4kC0sHeVe5QgUOR5YH0FPU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP934728.RA0ypCWf4wHof0VoEeDbenv4kC0sHeVe5QgUOR5YH0FPU130_assertion
a
np:Assertion
.
dgn-np:NP934728.RA0ypCWf4wHof0VoEeDbenv4kC0sHeVe5QgUOR5YH0FPU130_provenance
a
np:Provenance
.
dgn-np:NP934728.RA0ypCWf4wHof0VoEeDbenv4kC0sHeVe5QgUOR5YH0FPU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP934728.RA0ypCWf4wHof0VoEeDbenv4kC0sHeVe5QgUOR5YH0FPU130_assertion
{
miriam-gene:1236
a
ncit:C16612
.
lld:C1527336
a
ncit:C7057
.
dgn-gda:DGN354ea99ff0ddc501d5262ecae4402a5d
sio:SIO_000628
miriam-gene:1236
,
lld:C1527336
;
a
sio:SIO_001121
.
}
dgn-np:NP934728.RA0ypCWf4wHof0VoEeDbenv4kC0sHeVe5QgUOR5YH0FPU130_provenance
{
dgn-np:NP934728.RA0ypCWf4wHof0VoEeDbenv4kC0sHeVe5QgUOR5YH0FPU130_assertion
dcterms:description
"[These results suggest that variants of CCR7 gene occur at an extremely low frequency in the German population and that neither Sjogren's syndrome, systemic lupus erythematosus, nor systemic sclerosis are associated with these variants.]. 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:17587445
;
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:NP934728.RA0ypCWf4wHof0VoEeDbenv4kC0sHeVe5QgUOR5YH0FPU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:33+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" .
}