@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP894550.RAgQtXiAmQJcDGqWZapCFN7KXqRJN42BKGefpMz04ognk
> .
@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:NP894550.RAgQtXiAmQJcDGqWZapCFN7KXqRJN42BKGefpMz04ognk130_head
{
this:
np:hasAssertion
dgn-np:NP894550.RAgQtXiAmQJcDGqWZapCFN7KXqRJN42BKGefpMz04ognk130_assertion
;
np:hasProvenance
dgn-np:NP894550.RAgQtXiAmQJcDGqWZapCFN7KXqRJN42BKGefpMz04ognk130_provenance
;
np:hasPublicationInfo
dgn-np:NP894550.RAgQtXiAmQJcDGqWZapCFN7KXqRJN42BKGefpMz04ognk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP894550.RAgQtXiAmQJcDGqWZapCFN7KXqRJN42BKGefpMz04ognk130_assertion
a
np:Assertion
.
dgn-np:NP894550.RAgQtXiAmQJcDGqWZapCFN7KXqRJN42BKGefpMz04ognk130_provenance
a
np:Provenance
.
dgn-np:NP894550.RAgQtXiAmQJcDGqWZapCFN7KXqRJN42BKGefpMz04ognk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP894550.RAgQtXiAmQJcDGqWZapCFN7KXqRJN42BKGefpMz04ognk130_assertion
{
miriam-gene:23446
a
ncit:C16612
.
lld:C0524851
a
ncit:C7057
.
dgn-gda:DGNb5bac142a68a4ca1a497e5ce55ef1a39
sio:SIO_000628
miriam-gene:23446
,
lld:C0524851
;
a
sio:SIO_001121
.
}
dgn-np:NP894550.RAgQtXiAmQJcDGqWZapCFN7KXqRJN42BKGefpMz04ognk130_provenance
{
dgn-np:NP894550.RAgQtXiAmQJcDGqWZapCFN7KXqRJN42BKGefpMz04ognk130_assertion
dcterms:description
"[The presence of CTL1 protein in rat and human CNS regions, where it is found in neuronal, glial and endothelial cells, suggests that malfunction of this transporter could have important implications in nervous system development and repair following injury, and in neurodegenerative diseases.]. 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:19519661
;
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:NP894550.RAgQtXiAmQJcDGqWZapCFN7KXqRJN42BKGefpMz04ognk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:10+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" .
}