@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP766379.RA3dzo2wLz8aznfeMkJlsucBNy2b2YJrjggNzvZ83blcU
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP766379.RA3dzo2wLz8aznfeMkJlsucBNy2b2YJrjggNzvZ83blcU130_assertion
;
np:hasProvenance
dgn-np:NP766379.RA3dzo2wLz8aznfeMkJlsucBNy2b2YJrjggNzvZ83blcU130_provenance
;
np:hasPublicationInfo
dgn-np:NP766379.RA3dzo2wLz8aznfeMkJlsucBNy2b2YJrjggNzvZ83blcU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP766379.RA3dzo2wLz8aznfeMkJlsucBNy2b2YJrjggNzvZ83blcU130_assertion
a
np:Assertion
.
dgn-np:NP766379.RA3dzo2wLz8aznfeMkJlsucBNy2b2YJrjggNzvZ83blcU130_provenance
a
np:Provenance
.
dgn-np:NP766379.RA3dzo2wLz8aznfeMkJlsucBNy2b2YJrjggNzvZ83blcU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP766379.RA3dzo2wLz8aznfeMkJlsucBNy2b2YJrjggNzvZ83blcU130_assertion
{
miriam-gene:64127
a
ncit:C16612
.
lld:C0036202
a
ncit:C7057
.
dgn-gda:DGN1921f20609b8cc6cf9517efda08c82b0
sio:SIO_000628
miriam-gene:64127
,
lld:C0036202
;
a
sio:SIO_001121
.
}
dgn-np:NP766379.RA3dzo2wLz8aznfeMkJlsucBNy2b2YJrjggNzvZ83blcU130_provenance
{
dgn-np:NP766379.RA3dzo2wLz8aznfeMkJlsucBNy2b2YJrjggNzvZ83blcU130_assertion
dcterms:description
"[For the first time, an association between two CARD15 polymorphisms and specific sarcoidosis phenotypes has been demonstrated, as well as an additive effect of possessing CARD15 2104T and CCR5 HHC haplotype.]. 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:19679608
;
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:NP766379.RA3dzo2wLz8aznfeMkJlsucBNy2b2YJrjggNzvZ83blcU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:44+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" .
}