@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP833948.RArf2p88EpaUJAavBDBSEB3lm8R-BmYA680rNvUNs5jCA
> .
@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:NP833948.RArf2p88EpaUJAavBDBSEB3lm8R-BmYA680rNvUNs5jCA130_head
{
this:
np:hasAssertion
dgn-np:NP833948.RArf2p88EpaUJAavBDBSEB3lm8R-BmYA680rNvUNs5jCA130_assertion
;
np:hasProvenance
dgn-np:NP833948.RArf2p88EpaUJAavBDBSEB3lm8R-BmYA680rNvUNs5jCA130_provenance
;
np:hasPublicationInfo
dgn-np:NP833948.RArf2p88EpaUJAavBDBSEB3lm8R-BmYA680rNvUNs5jCA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP833948.RArf2p88EpaUJAavBDBSEB3lm8R-BmYA680rNvUNs5jCA130_assertion
a
np:Assertion
.
dgn-np:NP833948.RArf2p88EpaUJAavBDBSEB3lm8R-BmYA680rNvUNs5jCA130_provenance
a
np:Provenance
.
dgn-np:NP833948.RArf2p88EpaUJAavBDBSEB3lm8R-BmYA680rNvUNs5jCA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP833948.RArf2p88EpaUJAavBDBSEB3lm8R-BmYA680rNvUNs5jCA130_assertion
{
miriam-gene:2581
a
ncit:C16612
.
lld:C0037772
a
ncit:C7057
.
dgn-gda:DGNef419f12dada8dad0aadfee260f3218b
sio:SIO_000628
miriam-gene:2581
,
lld:C0037772
;
a
sio:SIO_001121
.
}
dgn-np:NP833948.RArf2p88EpaUJAavBDBSEB3lm8R-BmYA680rNvUNs5jCA130_provenance
{
dgn-np:NP833948.RArf2p88EpaUJAavBDBSEB3lm8R-BmYA680rNvUNs5jCA130_assertion
dcterms:description
"[We examined galactosylceramidase (GALC) cDNA in four Japanese patients with adult onset globoid cell leukodystrophy (Krabbe disease; AO-GLD) by polymerase chain reaction/single-strand conformation polymorphism (PCR-SSCP) analysis, subsequent sequence determination, and restriction enzyme digestion of PCR products, initial symptoms were the onset of slowly progressive spastic paraplegia from the middle of the second decade, and all patients had diminished GALC activity in their leukocytes.]. 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:9272171
;
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:NP833948.RArf2p88EpaUJAavBDBSEB3lm8R-BmYA680rNvUNs5jCA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:30+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" .
}