@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP573762.RAULyAKaacvr4_dkN_Eyb8XQpmDjsD2BrkOUD9PBLGGHM
> .
@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:NP573762.RAULyAKaacvr4_dkN_Eyb8XQpmDjsD2BrkOUD9PBLGGHM130_head
{
this:
np:hasAssertion
dgn-np:NP573762.RAULyAKaacvr4_dkN_Eyb8XQpmDjsD2BrkOUD9PBLGGHM130_assertion
;
np:hasProvenance
dgn-np:NP573762.RAULyAKaacvr4_dkN_Eyb8XQpmDjsD2BrkOUD9PBLGGHM130_provenance
;
np:hasPublicationInfo
dgn-np:NP573762.RAULyAKaacvr4_dkN_Eyb8XQpmDjsD2BrkOUD9PBLGGHM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP573762.RAULyAKaacvr4_dkN_Eyb8XQpmDjsD2BrkOUD9PBLGGHM130_assertion
a
np:Assertion
.
dgn-np:NP573762.RAULyAKaacvr4_dkN_Eyb8XQpmDjsD2BrkOUD9PBLGGHM130_provenance
a
np:Provenance
.
dgn-np:NP573762.RAULyAKaacvr4_dkN_Eyb8XQpmDjsD2BrkOUD9PBLGGHM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP573762.RAULyAKaacvr4_dkN_Eyb8XQpmDjsD2BrkOUD9PBLGGHM130_assertion
{
miriam-gene:2581
a
ncit:C16612
.
lld:C0085131
a
ncit:C7057
.
dgn-gda:DGN1c19b0eabc7868f0cc27cd4a9de24076
sio:SIO_000628
miriam-gene:2581
,
lld:C0085131
;
a
sio:SIO_001121
.
}
dgn-np:NP573762.RAULyAKaacvr4_dkN_Eyb8XQpmDjsD2BrkOUD9PBLGGHM130_provenance
{
dgn-np:NP573762.RAULyAKaacvr4_dkN_Eyb8XQpmDjsD2BrkOUD9PBLGGHM130_assertion
dcterms:description
"[In the galactosylceramide-loading tests using fibroblasts from patients with GLD and GM1 gangliosidosis, both cell lines hydrolyzed the incorporated galactosylceramide, with lower rates than control fibroblasts but higher than the fibroblasts from patients with I-cell disease, in which both galactosylceramidase I and II were deficient.]. 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:3934152
;
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:NP573762.RAULyAKaacvr4_dkN_Eyb8XQpmDjsD2BrkOUD9PBLGGHM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:46+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" .
}