@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP717664.RAv4ldH6AQGnverdWr2oiy3cEV4Yo8q93neuxdlXRA-kE
> .
@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:NP717664.RAv4ldH6AQGnverdWr2oiy3cEV4Yo8q93neuxdlXRA-kE130_head
{
this:
np:hasAssertion
dgn-np:NP717664.RAv4ldH6AQGnverdWr2oiy3cEV4Yo8q93neuxdlXRA-kE130_assertion
;
np:hasProvenance
dgn-np:NP717664.RAv4ldH6AQGnverdWr2oiy3cEV4Yo8q93neuxdlXRA-kE130_provenance
;
np:hasPublicationInfo
dgn-np:NP717664.RAv4ldH6AQGnverdWr2oiy3cEV4Yo8q93neuxdlXRA-kE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP717664.RAv4ldH6AQGnverdWr2oiy3cEV4Yo8q93neuxdlXRA-kE130_assertion
a
np:Assertion
.
dgn-np:NP717664.RAv4ldH6AQGnverdWr2oiy3cEV4Yo8q93neuxdlXRA-kE130_provenance
a
np:Provenance
.
dgn-np:NP717664.RAv4ldH6AQGnverdWr2oiy3cEV4Yo8q93neuxdlXRA-kE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP717664.RAv4ldH6AQGnverdWr2oiy3cEV4Yo8q93neuxdlXRA-kE130_assertion
{
miriam-gene:3561
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN2fa13bd00bfc7e809e0f7d66df013859
sio:SIO_000628
miriam-gene:3561
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP717664.RAv4ldH6AQGnverdWr2oiy3cEV4Yo8q93neuxdlXRA-kE130_provenance
{
dgn-np:NP717664.RAv4ldH6AQGnverdWr2oiy3cEV4Yo8q93neuxdlXRA-kE130_assertion
dcterms:description
"[Although many unique variables may have contributed to an increased risk in X-SCID patients, clonal dominance or frank neoplasia in animal models, clonal dominance in humans with chronic granulomatous disease, and the ability of retroviral integration to immortalize normal bone marrow cells or convert factor-dependent cells to factor independence suggest that transduction of cells with an integrating retrovirus has the potential for altering their subsequent biologic behavior.]. 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:16624621
;
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:NP717664.RAv4ldH6AQGnverdWr2oiy3cEV4Yo8q93neuxdlXRA-kE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:16+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" .
}