@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1197240.RALqvEuwEFzNVt5Eraf57W2NZdaMhQmxP29zKS1Rlxa_s
> .
@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/v4.0.0/void/
> .
dgn-np:NP1197240.RALqvEuwEFzNVt5Eraf57W2NZdaMhQmxP29zKS1Rlxa_s130_head
{
this:
np:hasAssertion
dgn-np:NP1197240.RALqvEuwEFzNVt5Eraf57W2NZdaMhQmxP29zKS1Rlxa_s130_assertion
;
np:hasProvenance
dgn-np:NP1197240.RALqvEuwEFzNVt5Eraf57W2NZdaMhQmxP29zKS1Rlxa_s130_provenance
;
np:hasPublicationInfo
dgn-np:NP1197240.RALqvEuwEFzNVt5Eraf57W2NZdaMhQmxP29zKS1Rlxa_s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1197240.RALqvEuwEFzNVt5Eraf57W2NZdaMhQmxP29zKS1Rlxa_s130_assertion
a
np:Assertion
.
dgn-np:NP1197240.RALqvEuwEFzNVt5Eraf57W2NZdaMhQmxP29zKS1Rlxa_s130_provenance
a
np:Provenance
.
dgn-np:NP1197240.RALqvEuwEFzNVt5Eraf57W2NZdaMhQmxP29zKS1Rlxa_s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1197240.RALqvEuwEFzNVt5Eraf57W2NZdaMhQmxP29zKS1Rlxa_s130_assertion
{
miriam-gene:1967
a
ncit:C16612
.
lld:C0270612
a
ncit:C7057
.
dgn-gda:DGN0d270810e0199cb356832393248578ac
sio:SIO_000628
miriam-gene:1967
,
lld:C0270612
;
a
sio:SIO_001121
.
}
dgn-np:NP1197240.RALqvEuwEFzNVt5Eraf57W2NZdaMhQmxP29zKS1Rlxa_s130_provenance
{
dgn-np:NP1197240.RALqvEuwEFzNVt5Eraf57W2NZdaMhQmxP29zKS1Rlxa_s130_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-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1197240.RALqvEuwEFzNVt5Eraf57W2NZdaMhQmxP29zKS1Rlxa_s130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:48+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}