@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP537730.RAPdQ9EgNc1ksku_iYca7QwAg0NPu5ReFlkqXE2ujKRAA
> .
@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:NP537730.RAPdQ9EgNc1ksku_iYca7QwAg0NPu5ReFlkqXE2ujKRAA130_head
{
this:
np:hasAssertion
dgn-np:NP537730.RAPdQ9EgNc1ksku_iYca7QwAg0NPu5ReFlkqXE2ujKRAA130_assertion
;
np:hasProvenance
dgn-np:NP537730.RAPdQ9EgNc1ksku_iYca7QwAg0NPu5ReFlkqXE2ujKRAA130_provenance
;
np:hasPublicationInfo
dgn-np:NP537730.RAPdQ9EgNc1ksku_iYca7QwAg0NPu5ReFlkqXE2ujKRAA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP537730.RAPdQ9EgNc1ksku_iYca7QwAg0NPu5ReFlkqXE2ujKRAA130_assertion
a
np:Assertion
.
dgn-np:NP537730.RAPdQ9EgNc1ksku_iYca7QwAg0NPu5ReFlkqXE2ujKRAA130_provenance
a
np:Provenance
.
dgn-np:NP537730.RAPdQ9EgNc1ksku_iYca7QwAg0NPu5ReFlkqXE2ujKRAA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP537730.RAPdQ9EgNc1ksku_iYca7QwAg0NPu5ReFlkqXE2ujKRAA130_assertion
{
miriam-gene:9219
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNd37644832ead5bb57c3f2cfa4d928f79
sio:SIO_000628
miriam-gene:9219
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP537730.RAPdQ9EgNc1ksku_iYca7QwAg0NPu5ReFlkqXE2ujKRAA130_provenance
{
dgn-np:NP537730.RAPdQ9EgNc1ksku_iYca7QwAg0NPu5ReFlkqXE2ujKRAA130_assertion
dcterms:description
"[Among them, hereditary diseases such as the primary immunodeficiency diseases (PID) were considered suitable candidates for gene therapy because the therapeutic strategy was very simple, therefore, effective gene therapy may be obtained without significant difficulty compared to other more complex diseases such as cancer.]. 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:16472146
;
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:NP537730.RAPdQ9EgNc1ksku_iYca7QwAg0NPu5ReFlkqXE2ujKRAA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:24+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" .
}