@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP810568.RAsORgayhOr8GiOExDc6Ot1sbzVA0jUZbUhAINp-7Sh-M
> .
@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:NP810568.RAsORgayhOr8GiOExDc6Ot1sbzVA0jUZbUhAINp-7Sh-M130_head
{
this:
np:hasAssertion
dgn-np:NP810568.RAsORgayhOr8GiOExDc6Ot1sbzVA0jUZbUhAINp-7Sh-M130_assertion
;
np:hasProvenance
dgn-np:NP810568.RAsORgayhOr8GiOExDc6Ot1sbzVA0jUZbUhAINp-7Sh-M130_provenance
;
np:hasPublicationInfo
dgn-np:NP810568.RAsORgayhOr8GiOExDc6Ot1sbzVA0jUZbUhAINp-7Sh-M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP810568.RAsORgayhOr8GiOExDc6Ot1sbzVA0jUZbUhAINp-7Sh-M130_assertion
a
np:Assertion
.
dgn-np:NP810568.RAsORgayhOr8GiOExDc6Ot1sbzVA0jUZbUhAINp-7Sh-M130_provenance
a
np:Provenance
.
dgn-np:NP810568.RAsORgayhOr8GiOExDc6Ot1sbzVA0jUZbUhAINp-7Sh-M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP810568.RAsORgayhOr8GiOExDc6Ot1sbzVA0jUZbUhAINp-7Sh-M130_assertion
{
miriam-gene:8894
a
ncit:C16612
.
lld:C0270612
a
ncit:C7057
.
dgn-gda:DGNee944e4a72ca80995fd3cb48a6ba4d00
sio:SIO_000628
miriam-gene:8894
,
lld:C0270612
;
a
sio:SIO_001121
.
}
dgn-np:NP810568.RAsORgayhOr8GiOExDc6Ot1sbzVA0jUZbUhAINp-7Sh-M130_provenance
{
dgn-np:NP810568.RAsORgayhOr8GiOExDc6Ot1sbzVA0jUZbUhAINp-7Sh-M130_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:NP810568.RAsORgayhOr8GiOExDc6Ot1sbzVA0jUZbUhAINp-7Sh-M130_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" .
}