@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP528979.RAibu3MSPjLLmgF32yP2TFKV_2Y9hLoF0L8m7X2jzKGXk
> .
@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:NP528979.RAibu3MSPjLLmgF32yP2TFKV_2Y9hLoF0L8m7X2jzKGXk130_head
{
this:
np:hasAssertion
dgn-np:NP528979.RAibu3MSPjLLmgF32yP2TFKV_2Y9hLoF0L8m7X2jzKGXk130_assertion
;
np:hasProvenance
dgn-np:NP528979.RAibu3MSPjLLmgF32yP2TFKV_2Y9hLoF0L8m7X2jzKGXk130_provenance
;
np:hasPublicationInfo
dgn-np:NP528979.RAibu3MSPjLLmgF32yP2TFKV_2Y9hLoF0L8m7X2jzKGXk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP528979.RAibu3MSPjLLmgF32yP2TFKV_2Y9hLoF0L8m7X2jzKGXk130_assertion
a
np:Assertion
.
dgn-np:NP528979.RAibu3MSPjLLmgF32yP2TFKV_2Y9hLoF0L8m7X2jzKGXk130_provenance
a
np:Provenance
.
dgn-np:NP528979.RAibu3MSPjLLmgF32yP2TFKV_2Y9hLoF0L8m7X2jzKGXk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP528979.RAibu3MSPjLLmgF32yP2TFKV_2Y9hLoF0L8m7X2jzKGXk130_assertion
{
miriam-gene:3561
a
ncit:C16612
.
lld:C0018203
a
ncit:C7057
.
dgn-gda:DGNe16e04a4bccf27e9660d829882a89099
sio:SIO_000628
miriam-gene:3561
,
lld:C0018203
;
a
sio:SIO_001121
.
}
dgn-np:NP528979.RAibu3MSPjLLmgF32yP2TFKV_2Y9hLoF0L8m7X2jzKGXk130_provenance
{
dgn-np:NP528979.RAibu3MSPjLLmgF32yP2TFKV_2Y9hLoF0L8m7X2jzKGXk130_assertion
dcterms:description
"[A series of encouraging results obtained in chronic granulomatous disease (CGD) patients have followed these pioneer experiments and preceded the very recent and exciting reports of successful genetic correction procedures performed in patients affected with the X-linked form of severe combined immunodeficiency (XSCID).]. 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:11892066
;
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:NP528979.RAibu3MSPjLLmgF32yP2TFKV_2Y9hLoF0L8m7X2jzKGXk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:19+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" .
}