@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP203244.RAo-Nshvv4bjk1X0D9rXyhLgiAhPPk-TurHuYdRPPe9jI
> .
@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:NP203244.RAo-Nshvv4bjk1X0D9rXyhLgiAhPPk-TurHuYdRPPe9jI130_head
{
this:
np:hasAssertion
dgn-np:NP203244.RAo-Nshvv4bjk1X0D9rXyhLgiAhPPk-TurHuYdRPPe9jI130_assertion
;
np:hasProvenance
dgn-np:NP203244.RAo-Nshvv4bjk1X0D9rXyhLgiAhPPk-TurHuYdRPPe9jI130_provenance
;
np:hasPublicationInfo
dgn-np:NP203244.RAo-Nshvv4bjk1X0D9rXyhLgiAhPPk-TurHuYdRPPe9jI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP203244.RAo-Nshvv4bjk1X0D9rXyhLgiAhPPk-TurHuYdRPPe9jI130_assertion
a
np:Assertion
.
dgn-np:NP203244.RAo-Nshvv4bjk1X0D9rXyhLgiAhPPk-TurHuYdRPPe9jI130_provenance
a
np:Provenance
.
dgn-np:NP203244.RAo-Nshvv4bjk1X0D9rXyhLgiAhPPk-TurHuYdRPPe9jI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP203244.RAo-Nshvv4bjk1X0D9rXyhLgiAhPPk-TurHuYdRPPe9jI130_assertion
{
miriam-gene:3561
a
ncit:C16612
.
lld:C2931540
a
ncit:C7057
.
dgn-gda:DGNbe52fec323e4dff8bbe71c7e2ad778db
sio:SIO_000628
miriam-gene:3561
,
lld:C2931540
;
a
sio:SIO_001121
.
}
dgn-np:NP203244.RAo-Nshvv4bjk1X0D9rXyhLgiAhPPk-TurHuYdRPPe9jI130_provenance
{
dgn-np:NP203244.RAo-Nshvv4bjk1X0D9rXyhLgiAhPPk-TurHuYdRPPe9jI130_assertion
dcterms:description
"[In this study, an MND-IL-2R vector containing IL-2Rc gamma cDNA to treat X-linked severe combined immunodeficiency (X-SCID) was constructed from an MND vector that was modified by substituting the myeloproliferative sarcoma virus (MPSV) enhancer for that of MoMLV, deleting the negative control region located in the long terminal repeat (LTR) as an enhancer, and replacing the primer binding site (PBS) of MoMLV with the PBS of the endogenous murine retrovirus dl587rev.]. 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:15129596
;
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:NP203244.RAo-Nshvv4bjk1X0D9rXyhLgiAhPPk-TurHuYdRPPe9jI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:52+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" .
}