@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP905363.RAILAKfJwOLOMqP4euBMNCF78z3ufUD-BHBJZ_IMY36eE
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP905363.RAILAKfJwOLOMqP4euBMNCF78z3ufUD-BHBJZ_IMY36eE130_head
{
this:
np:hasAssertion
dgn-np:NP905363.RAILAKfJwOLOMqP4euBMNCF78z3ufUD-BHBJZ_IMY36eE130_assertion
;
np:hasProvenance
dgn-np:NP905363.RAILAKfJwOLOMqP4euBMNCF78z3ufUD-BHBJZ_IMY36eE130_provenance
;
np:hasPublicationInfo
dgn-np:NP905363.RAILAKfJwOLOMqP4euBMNCF78z3ufUD-BHBJZ_IMY36eE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP905363.RAILAKfJwOLOMqP4euBMNCF78z3ufUD-BHBJZ_IMY36eE130_assertion
a
np:Assertion
.
dgn-np:NP905363.RAILAKfJwOLOMqP4euBMNCF78z3ufUD-BHBJZ_IMY36eE130_provenance
a
np:Provenance
.
dgn-np:NP905363.RAILAKfJwOLOMqP4euBMNCF78z3ufUD-BHBJZ_IMY36eE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP905363.RAILAKfJwOLOMqP4euBMNCF78z3ufUD-BHBJZ_IMY36eE130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGNe9f62c667e4c3553155ebc5726f1017b
sio:SIO_000628
miriam-gene:4397
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP905363.RAILAKfJwOLOMqP4euBMNCF78z3ufUD-BHBJZ_IMY36eE130_provenance
{
dgn-np:NP905363.RAILAKfJwOLOMqP4euBMNCF78z3ufUD-BHBJZ_IMY36eE130_assertion
dcterms:description
"[The picture that emerges from the studies described suggests that although schizophrenia is not characterized by gross abnormalities of white matter such as those evident in multiple sclerosis, it does involve a profound dysregulation of myelin-associated gene expression, reductions in oligodendrocyte numbers, and marked abnormalities in the ultrastructure of myelin sheaths.]. 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:17583597
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP905363.RAILAKfJwOLOMqP4euBMNCF78z3ufUD-BHBJZ_IMY36eE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:16+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}