@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP755087.RApO2ybAqv8a9s4X2G6AjCYX8mRUc7D9uMdjF0BGn9cqw
> .
@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:NP755087.RApO2ybAqv8a9s4X2G6AjCYX8mRUc7D9uMdjF0BGn9cqw130_head
{
this:
np:hasAssertion
dgn-np:NP755087.RApO2ybAqv8a9s4X2G6AjCYX8mRUc7D9uMdjF0BGn9cqw130_assertion
;
np:hasProvenance
dgn-np:NP755087.RApO2ybAqv8a9s4X2G6AjCYX8mRUc7D9uMdjF0BGn9cqw130_provenance
;
np:hasPublicationInfo
dgn-np:NP755087.RApO2ybAqv8a9s4X2G6AjCYX8mRUc7D9uMdjF0BGn9cqw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP755087.RApO2ybAqv8a9s4X2G6AjCYX8mRUc7D9uMdjF0BGn9cqw130_assertion
a
np:Assertion
.
dgn-np:NP755087.RApO2ybAqv8a9s4X2G6AjCYX8mRUc7D9uMdjF0BGn9cqw130_provenance
a
np:Provenance
.
dgn-np:NP755087.RApO2ybAqv8a9s4X2G6AjCYX8mRUc7D9uMdjF0BGn9cqw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP755087.RApO2ybAqv8a9s4X2G6AjCYX8mRUc7D9uMdjF0BGn9cqw130_assertion
{
miriam-gene:6387
a
ncit:C16612
.
lld:C0272173
a
ncit:C7057
.
dgn-gda:DGN0f0fd27c10215cfb138080ecbcdeb093
sio:SIO_000628
miriam-gene:6387
,
lld:C0272173
;
a
sio:SIO_001121
.
}
dgn-np:NP755087.RApO2ybAqv8a9s4X2G6AjCYX8mRUc7D9uMdjF0BGn9cqw130_provenance
{
dgn-np:NP755087.RApO2ybAqv8a9s4X2G6AjCYX8mRUc7D9uMdjF0BGn9cqw130_assertion
dcterms:description
"[Based on our results, we suggest that the altered leukocyte response to CXCL12 may account for the pathologic retention of mature polymorphonuclear cells in the bone marrow (myelokathexis) and for an altered lymphocyte trafficking, which may cause the immunophenotyping abnormalities observed in WHIM patients.]. 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:15026312
;
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:NP755087.RApO2ybAqv8a9s4X2G6AjCYX8mRUc7D9uMdjF0BGn9cqw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:37+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" .
}