@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP810476.RAhJHrnFpAfoJXaN5UuPNXqJK8pxkbkO9Njg8kPWazV78
> .
@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:NP810476.RAhJHrnFpAfoJXaN5UuPNXqJK8pxkbkO9Njg8kPWazV78130_head
{
this:
np:hasAssertion
dgn-np:NP810476.RAhJHrnFpAfoJXaN5UuPNXqJK8pxkbkO9Njg8kPWazV78130_assertion
;
np:hasProvenance
dgn-np:NP810476.RAhJHrnFpAfoJXaN5UuPNXqJK8pxkbkO9Njg8kPWazV78130_provenance
;
np:hasPublicationInfo
dgn-np:NP810476.RAhJHrnFpAfoJXaN5UuPNXqJK8pxkbkO9Njg8kPWazV78130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP810476.RAhJHrnFpAfoJXaN5UuPNXqJK8pxkbkO9Njg8kPWazV78130_assertion
a
np:Assertion
.
dgn-np:NP810476.RAhJHrnFpAfoJXaN5UuPNXqJK8pxkbkO9Njg8kPWazV78130_provenance
a
np:Provenance
.
dgn-np:NP810476.RAhJHrnFpAfoJXaN5UuPNXqJK8pxkbkO9Njg8kPWazV78130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP810476.RAhJHrnFpAfoJXaN5UuPNXqJK8pxkbkO9Njg8kPWazV78130_assertion
{
miriam-gene:8892
a
ncit:C16612
.
lld:C0747102
a
ncit:C7057
.
dgn-gda:DGNd15fa581f20453001e88eca59405a97e
sio:SIO_000628
miriam-gene:8892
,
lld:C0747102
;
a
sio:SIO_001121
.
}
dgn-np:NP810476.RAhJHrnFpAfoJXaN5UuPNXqJK8pxkbkO9Njg8kPWazV78130_provenance
{
dgn-np:NP810476.RAhJHrnFpAfoJXaN5UuPNXqJK8pxkbkO9Njg8kPWazV78130_assertion
dcterms:description
"[It is surprising that mutations in the eIF2B genes have been reported to lead to abnormalities of the white matter of the brain only, although it has been shown recently that ovarian failure may accompany the leukoencephalopathy.]. 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:14566705
;
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:NP810476.RAhJHrnFpAfoJXaN5UuPNXqJK8pxkbkO9Njg8kPWazV78130_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" .
}