@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY
> .
@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:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_head
{
this:
np:hasAssertion
dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_assertion
;
np:hasProvenance
dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_provenance
;
np:hasPublicationInfo
dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_assertion
a
np:Assertion
.
dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_provenance
a
np:Provenance
.
dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_assertion
{
miriam-gene:3918
a
ncit:C16612
.
lld:C1458156
a
ncit:C7057
.
dgn-gda:DGNcca661ce4562390925d60c2149d85250
sio:SIO_000628
miriam-gene:3918
,
lld:C1458156
;
a
sio:SIO_001121
.
}
dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_provenance
{
dgn-np:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_assertion
dcterms:description
"[The PNET may be amenable in the future to gene therapy strategies because of its rapid proliferative potential, its tendency to spread within the CSF pathways, and its high recurrence rate.]. 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:8817422
;
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:NP876106.RA8yu5FArNKW8dHSkpfQ4RhXiH4Obel-fcKQRspCo2wGY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:55+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" .
}