@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP810468.RAFzQOgVyf4V52R9BUkDz04NeD-0sBePCB0UR9geSFq8c
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP810468.RAFzQOgVyf4V52R9BUkDz04NeD-0sBePCB0UR9geSFq8c130_head
{
this:
np:hasAssertion
dgn-np:NP810468.RAFzQOgVyf4V52R9BUkDz04NeD-0sBePCB0UR9geSFq8c130_assertion
;
np:hasProvenance
dgn-np:NP810468.RAFzQOgVyf4V52R9BUkDz04NeD-0sBePCB0UR9geSFq8c130_provenance
;
np:hasPublicationInfo
dgn-np:NP810468.RAFzQOgVyf4V52R9BUkDz04NeD-0sBePCB0UR9geSFq8c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP810468.RAFzQOgVyf4V52R9BUkDz04NeD-0sBePCB0UR9geSFq8c130_assertion
a
np:Assertion
.
dgn-np:NP810468.RAFzQOgVyf4V52R9BUkDz04NeD-0sBePCB0UR9geSFq8c130_provenance
a
np:Provenance
.
dgn-np:NP810468.RAFzQOgVyf4V52R9BUkDz04NeD-0sBePCB0UR9geSFq8c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP810468.RAFzQOgVyf4V52R9BUkDz04NeD-0sBePCB0UR9geSFq8c130_assertion
{
miriam-gene:8892
a
ncit:C16612
.
lld:C0270612
a
ncit:C7057
.
dgn-gda:DGNdd8a3ce62a7934a5b6222bb2bf7bde12
sio:SIO_000628
miriam-gene:8892
,
lld:C0270612
;
a
sio:SIO_001121
.
}
dgn-np:NP810468.RAFzQOgVyf4V52R9BUkDz04NeD-0sBePCB0UR9geSFq8c130_provenance
{
dgn-np:NP810468.RAFzQOgVyf4V52R9BUkDz04NeD-0sBePCB0UR9geSFq8c130_assertion
dcterms:description
"[The previous studies have shown that mutations in five subunits of eIF2B cause white matter disease of the brain and thus EIF2B is the main culprit in development of white matter disease.]. 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:24980014
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP810468.RAFzQOgVyf4V52R9BUkDz04NeD-0sBePCB0UR9geSFq8c130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:51+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}