@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP785190.RAN0jMGBeUGfrXq_cnwa7o9HHOmGGpVUYGkWvggcaW7L8
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP785190.RAN0jMGBeUGfrXq_cnwa7o9HHOmGGpVUYGkWvggcaW7L8130_head
{
this:
np:hasAssertion
dgn-np:NP785190.RAN0jMGBeUGfrXq_cnwa7o9HHOmGGpVUYGkWvggcaW7L8130_assertion
;
np:hasProvenance
dgn-np:NP785190.RAN0jMGBeUGfrXq_cnwa7o9HHOmGGpVUYGkWvggcaW7L8130_provenance
;
np:hasPublicationInfo
dgn-np:NP785190.RAN0jMGBeUGfrXq_cnwa7o9HHOmGGpVUYGkWvggcaW7L8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP785190.RAN0jMGBeUGfrXq_cnwa7o9HHOmGGpVUYGkWvggcaW7L8130_assertion
a
np:Assertion
.
dgn-np:NP785190.RAN0jMGBeUGfrXq_cnwa7o9HHOmGGpVUYGkWvggcaW7L8130_provenance
a
np:Provenance
.
dgn-np:NP785190.RAN0jMGBeUGfrXq_cnwa7o9HHOmGGpVUYGkWvggcaW7L8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP785190.RAN0jMGBeUGfrXq_cnwa7o9HHOmGGpVUYGkWvggcaW7L8130_assertion
{
miriam-gene:7852
a
ncit:C16612
.
lld:C0746882
a
ncit:C7057
.
dgn-gda:DGN2fb0baad7e9b08ab480adc6e7ef461c6
sio:SIO_000628
miriam-gene:7852
,
lld:C0746882
;
a
sio:SIO_001121
.
}
dgn-np:NP785190.RAN0jMGBeUGfrXq_cnwa7o9HHOmGGpVUYGkWvggcaW7L8130_provenance
{
dgn-np:NP785190.RAN0jMGBeUGfrXq_cnwa7o9HHOmGGpVUYGkWvggcaW7L8130_assertion
dcterms:description
"[The mutated gene may result in production of the mutant CXCR4 protein causing abnormal apoptosis and migratory function, which are thought to be related to the cause of chronic neutropenia in WHIM syndrome.]. 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:16154852
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP785190.RAN0jMGBeUGfrXq_cnwa7o9HHOmGGpVUYGkWvggcaW7L8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:34+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}