@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP587709.RAWNHL5VS6YO59twhTELxfKj1sYjDHfOezzl71qxAgnIA
> .
@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:NP587709.RAWNHL5VS6YO59twhTELxfKj1sYjDHfOezzl71qxAgnIA130_head
{
this:
np:hasAssertion
dgn-np:NP587709.RAWNHL5VS6YO59twhTELxfKj1sYjDHfOezzl71qxAgnIA130_assertion
;
np:hasProvenance
dgn-np:NP587709.RAWNHL5VS6YO59twhTELxfKj1sYjDHfOezzl71qxAgnIA130_provenance
;
np:hasPublicationInfo
dgn-np:NP587709.RAWNHL5VS6YO59twhTELxfKj1sYjDHfOezzl71qxAgnIA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP587709.RAWNHL5VS6YO59twhTELxfKj1sYjDHfOezzl71qxAgnIA130_assertion
a
np:Assertion
.
dgn-np:NP587709.RAWNHL5VS6YO59twhTELxfKj1sYjDHfOezzl71qxAgnIA130_provenance
a
np:Provenance
.
dgn-np:NP587709.RAWNHL5VS6YO59twhTELxfKj1sYjDHfOezzl71qxAgnIA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP587709.RAWNHL5VS6YO59twhTELxfKj1sYjDHfOezzl71qxAgnIA130_assertion
{
miriam-gene:2581
a
ncit:C16612
.
lld:C0011303
a
ncit:C7057
.
dgn-gda:DGNf57f795da648fecb1e599763a8ef4d4c
sio:SIO_000628
miriam-gene:2581
,
lld:C0011303
;
a
sio:SIO_001121
.
}
dgn-np:NP587709.RAWNHL5VS6YO59twhTELxfKj1sYjDHfOezzl71qxAgnIA130_provenance
{
dgn-np:NP587709.RAWNHL5VS6YO59twhTELxfKj1sYjDHfOezzl71qxAgnIA130_assertion
dcterms:description
"[Krabbe's disease or globoid cell leukodystrophy is a rare demyelinating disorder of the central and peripheral nervous systems, the diagnosis of which is based on clinical findings and the determination of low to absent functional activity of the enzyme beta-galactocerebrosidase.]. 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:9005874
;
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:NP587709.RAWNHL5VS6YO59twhTELxfKj1sYjDHfOezzl71qxAgnIA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}