@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP841312.RATWARY6FvCdOVX72C907Ah-cbKg8J6uLgdpu9bmKG26s
> .
@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:NP841312.RATWARY6FvCdOVX72C907Ah-cbKg8J6uLgdpu9bmKG26s130_head
{
this:
np:hasAssertion
dgn-np:NP841312.RATWARY6FvCdOVX72C907Ah-cbKg8J6uLgdpu9bmKG26s130_assertion
;
np:hasProvenance
dgn-np:NP841312.RATWARY6FvCdOVX72C907Ah-cbKg8J6uLgdpu9bmKG26s130_provenance
;
np:hasPublicationInfo
dgn-np:NP841312.RATWARY6FvCdOVX72C907Ah-cbKg8J6uLgdpu9bmKG26s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP841312.RATWARY6FvCdOVX72C907Ah-cbKg8J6uLgdpu9bmKG26s130_assertion
a
np:Assertion
.
dgn-np:NP841312.RATWARY6FvCdOVX72C907Ah-cbKg8J6uLgdpu9bmKG26s130_provenance
a
np:Provenance
.
dgn-np:NP841312.RATWARY6FvCdOVX72C907Ah-cbKg8J6uLgdpu9bmKG26s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP841312.RATWARY6FvCdOVX72C907Ah-cbKg8J6uLgdpu9bmKG26s130_assertion
{
miriam-gene:81704
a
ncit:C16612
.
lld:C0494261
a
ncit:C7057
.
dgn-gda:DGN5786e9f16748af24db70dd82e9411476
sio:SIO_000628
miriam-gene:81704
,
lld:C0494261
;
a
sio:SIO_001121
.
}
dgn-np:NP841312.RATWARY6FvCdOVX72C907Ah-cbKg8J6uLgdpu9bmKG26s130_provenance
{
dgn-np:NP841312.RATWARY6FvCdOVX72C907Ah-cbKg8J6uLgdpu9bmKG26s130_assertion
dcterms:description
"[Dedicator of cytokinesis 8 protein (DOCK8) deficiency is a combined immunodeficiency disorder characterized by an expanding clinical picture with typical features of recurrent respiratory or gastrointestinal tract infections, atopic eczema, food allergies, chronic viral infections of the skin, and blood eosinophilia often accompanied by elevated serum IgE levels.]. 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:22897717
;
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:NP841312.RATWARY6FvCdOVX72C907Ah-cbKg8J6uLgdpu9bmKG26s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:34+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" .
}