@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP810580.RAcN_iAA56O0OfKlIA5mCBeG2t_l9kzz9FeS7JIvKNZxg
> .
@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:NP810580.RAcN_iAA56O0OfKlIA5mCBeG2t_l9kzz9FeS7JIvKNZxg130_head
{
this:
np:hasAssertion
dgn-np:NP810580.RAcN_iAA56O0OfKlIA5mCBeG2t_l9kzz9FeS7JIvKNZxg130_assertion
;
np:hasProvenance
dgn-np:NP810580.RAcN_iAA56O0OfKlIA5mCBeG2t_l9kzz9FeS7JIvKNZxg130_provenance
;
np:hasPublicationInfo
dgn-np:NP810580.RAcN_iAA56O0OfKlIA5mCBeG2t_l9kzz9FeS7JIvKNZxg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP810580.RAcN_iAA56O0OfKlIA5mCBeG2t_l9kzz9FeS7JIvKNZxg130_assertion
a
np:Assertion
.
dgn-np:NP810580.RAcN_iAA56O0OfKlIA5mCBeG2t_l9kzz9FeS7JIvKNZxg130_provenance
a
np:Provenance
.
dgn-np:NP810580.RAcN_iAA56O0OfKlIA5mCBeG2t_l9kzz9FeS7JIvKNZxg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP810580.RAcN_iAA56O0OfKlIA5mCBeG2t_l9kzz9FeS7JIvKNZxg130_assertion
{
miriam-gene:8894
a
ncit:C16612
.
lld:C0747102
a
ncit:C7057
.
dgn-gda:DGN87c1331bd6f767e66383832fc599e05d
sio:SIO_000628
miriam-gene:8894
,
lld:C0747102
;
a
sio:SIO_001121
.
}
dgn-np:NP810580.RAcN_iAA56O0OfKlIA5mCBeG2t_l9kzz9FeS7JIvKNZxg130_provenance
{
dgn-np:NP810580.RAcN_iAA56O0OfKlIA5mCBeG2t_l9kzz9FeS7JIvKNZxg130_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:NP810580.RAcN_iAA56O0OfKlIA5mCBeG2t_l9kzz9FeS7JIvKNZxg130_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" .
}