@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP707408.RAekB0N9UXANVNzbZk251wj8LFUhHajUCgI_PpG-nqtlA
> .
@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/v4.0.0/void/
> .
dgn-np:NP707408.RAekB0N9UXANVNzbZk251wj8LFUhHajUCgI_PpG-nqtlA130_head
{
this:
np:hasAssertion
dgn-np:NP707408.RAekB0N9UXANVNzbZk251wj8LFUhHajUCgI_PpG-nqtlA130_assertion
;
np:hasProvenance
dgn-np:NP707408.RAekB0N9UXANVNzbZk251wj8LFUhHajUCgI_PpG-nqtlA130_provenance
;
np:hasPublicationInfo
dgn-np:NP707408.RAekB0N9UXANVNzbZk251wj8LFUhHajUCgI_PpG-nqtlA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP707408.RAekB0N9UXANVNzbZk251wj8LFUhHajUCgI_PpG-nqtlA130_assertion
a
np:Assertion
.
dgn-np:NP707408.RAekB0N9UXANVNzbZk251wj8LFUhHajUCgI_PpG-nqtlA130_provenance
a
np:Provenance
.
dgn-np:NP707408.RAekB0N9UXANVNzbZk251wj8LFUhHajUCgI_PpG-nqtlA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP707408.RAekB0N9UXANVNzbZk251wj8LFUhHajUCgI_PpG-nqtlA130_assertion
{
miriam-gene:7852
a
ncit:C16612
.
lld:C0472817
a
ncit:C7057
.
dgn-gda:DGN5614a8eab4f918406d60ccdd60377e90
sio:SIO_000628
miriam-gene:7852
,
lld:C0472817
;
a
sio:SIO_001121
.
}
dgn-np:NP707408.RAekB0N9UXANVNzbZk251wj8LFUhHajUCgI_PpG-nqtlA130_provenance
{
dgn-np:NP707408.RAekB0N9UXANVNzbZk251wj8LFUhHajUCgI_PpG-nqtlA130_assertion
dcterms:description
"[Finding two patients with WHIM who do not have detectable mutations of CXCR4 but whose cells are hyperresponsive to CXCL12 raises the possibility that there is more than one genetic basis for WHIM.]. 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:19057201
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP707408.RAekB0N9UXANVNzbZk251wj8LFUhHajUCgI_PpG-nqtlA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:05+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}