@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP695769.RAmvlfLCBBTaim2aFsEO6LLOQ9kQdAsLaIisjtcQ5fv9A
> .
@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:NP695769.RAmvlfLCBBTaim2aFsEO6LLOQ9kQdAsLaIisjtcQ5fv9A130_head
{
this:
np:hasAssertion
dgn-np:NP695769.RAmvlfLCBBTaim2aFsEO6LLOQ9kQdAsLaIisjtcQ5fv9A130_assertion
;
np:hasProvenance
dgn-np:NP695769.RAmvlfLCBBTaim2aFsEO6LLOQ9kQdAsLaIisjtcQ5fv9A130_provenance
;
np:hasPublicationInfo
dgn-np:NP695769.RAmvlfLCBBTaim2aFsEO6LLOQ9kQdAsLaIisjtcQ5fv9A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP695769.RAmvlfLCBBTaim2aFsEO6LLOQ9kQdAsLaIisjtcQ5fv9A130_assertion
a
np:Assertion
.
dgn-np:NP695769.RAmvlfLCBBTaim2aFsEO6LLOQ9kQdAsLaIisjtcQ5fv9A130_provenance
a
np:Provenance
.
dgn-np:NP695769.RAmvlfLCBBTaim2aFsEO6LLOQ9kQdAsLaIisjtcQ5fv9A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP695769.RAmvlfLCBBTaim2aFsEO6LLOQ9kQdAsLaIisjtcQ5fv9A130_assertion
{
miriam-gene:2670
a
ncit:C16612
.
lld:C0027873
a
ncit:C7057
.
dgn-gda:DGN0a0b04f66e7a9edffdeab034fc928969
sio:SIO_000628
miriam-gene:2670
,
lld:C0027873
;
a
sio:SIO_001121
.
}
dgn-np:NP695769.RAmvlfLCBBTaim2aFsEO6LLOQ9kQdAsLaIisjtcQ5fv9A130_provenance
{
dgn-np:NP695769.RAmvlfLCBBTaim2aFsEO6LLOQ9kQdAsLaIisjtcQ5fv9A130_assertion
dcterms:description
"[We evaluated AQP4 expression relative to glial fibrillary acidic protein, extent of demyelination, lesion staging (CD68 staining for macrophages), and perivascular deposition of complement and immunoglobulin in 11 cases with NMO and NMO spectrum disorders (NMOSD), five with MS and 30 with other neurological diseases.]. 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:21241398
;
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:NP695769.RAmvlfLCBBTaim2aFsEO6LLOQ9kQdAsLaIisjtcQ5fv9A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:03+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" .
}