@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP1960.RASjo8yDYqiEYAX3I9BntiVZZILDuSTijovgnxEhYo1Zg
> .
@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 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:NP1960.RASjo8yDYqiEYAX3I9BntiVZZILDuSTijovgnxEhYo1Zg130_head
{
this:
np:hasAssertion
dgn-np:NP1960.RASjo8yDYqiEYAX3I9BntiVZZILDuSTijovgnxEhYo1Zg130_assertion
;
np:hasProvenance
dgn-np:NP1960.RASjo8yDYqiEYAX3I9BntiVZZILDuSTijovgnxEhYo1Zg130_provenance
;
np:hasPublicationInfo
dgn-np:NP1960.RASjo8yDYqiEYAX3I9BntiVZZILDuSTijovgnxEhYo1Zg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1960.RASjo8yDYqiEYAX3I9BntiVZZILDuSTijovgnxEhYo1Zg130_assertion
a
np:Assertion
.
dgn-np:NP1960.RASjo8yDYqiEYAX3I9BntiVZZILDuSTijovgnxEhYo1Zg130_provenance
a
np:Provenance
.
dgn-np:NP1960.RASjo8yDYqiEYAX3I9BntiVZZILDuSTijovgnxEhYo1Zg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1960.RASjo8yDYqiEYAX3I9BntiVZZILDuSTijovgnxEhYo1Zg130_assertion
{
miriam-gene:8893
a
ncit:C16612
.
lld:C1858991
a
ncit:C7057
.
dgn-gda:DGN4059ea0492623ad7961f59d8a8728778
sio:SIO_000628
miriam-gene:8893
,
lld:C1858991
;
a
sio:SIO_001122
.
}
dgn-np:NP1960.RASjo8yDYqiEYAX3I9BntiVZZILDuSTijovgnxEhYo1Zg130_provenance
{
dgn-np:NP1960.RASjo8yDYqiEYAX3I9BntiVZZILDuSTijovgnxEhYo1Zg130_assertion
dct:description
"[In this study 15 well-characterised patients with the classical form of leukoencephalopathy with vanishing white matter (VWM) or with phenotypic variants like ovarioleukodystrophy were investigated for mutations in the genes EIF2B1, EIF2B2, EIF2B3, EIF2B4, and EIF2B5 encoding eIF2B.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:15776425
;
prov:wasDerivedFrom
dgn-void:uniprot-20130724
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
dgn-void:uniprot-20130724
pav:importedOn
"2013-07-24"^^
xsd:date
.
}
dgn-np:NP1960.RASjo8yDYqiEYAX3I9BntiVZZILDuSTijovgnxEhYo1Zg130_publicationInfo
{
this:
dct:created
"2014-10-02T12:31:58+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}