@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA
> .
@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:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_head
{
this:
np:hasAssertion
dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_assertion
;
np:hasProvenance
dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_provenance
;
np:hasPublicationInfo
dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_assertion
a
np:Assertion
.
dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_provenance
a
np:Provenance
.
dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_assertion
{
miriam-gene:410
a
ncit:C16612
.
lld:C0268547
a
ncit:C7057
.
dgn-gda:DGNc14a03f2095c39114a19434bc6c808dc
sio:SIO_000628
miriam-gene:410
,
lld:C0268547
;
a
sio:SIO_001121
.
}
dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_provenance
{
dgn-np:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_assertion
dcterms:description
"[It was concluded that the correction of ASA deficiency by a recombinant adenovirus that potentially could be used to transfer the gene to the brain, and gene therapy for MLD based on gene transfer of the ASA gene to mutant cells will be feasible because the overexpression of ASA in cells does not lead to profound deficiency of other sulfatases or result in a new phenotype.]. 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:8677802
;
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:NP506050.RAZy2xXpZLp0uB6oS0LQ_XegbAG4wZ1TPZ-gSLG0HGGCA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:02+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" .
}