@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP806069.RAWYjCyzmzNzZkhnrJ9dBxpGAI3V9lDROB112UJo_sqG8
> .
@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:NP806069.RAWYjCyzmzNzZkhnrJ9dBxpGAI3V9lDROB112UJo_sqG8130_head
{
this:
np:hasAssertion
dgn-np:NP806069.RAWYjCyzmzNzZkhnrJ9dBxpGAI3V9lDROB112UJo_sqG8130_assertion
;
np:hasProvenance
dgn-np:NP806069.RAWYjCyzmzNzZkhnrJ9dBxpGAI3V9lDROB112UJo_sqG8130_provenance
;
np:hasPublicationInfo
dgn-np:NP806069.RAWYjCyzmzNzZkhnrJ9dBxpGAI3V9lDROB112UJo_sqG8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP806069.RAWYjCyzmzNzZkhnrJ9dBxpGAI3V9lDROB112UJo_sqG8130_assertion
a
np:Assertion
.
dgn-np:NP806069.RAWYjCyzmzNzZkhnrJ9dBxpGAI3V9lDROB112UJo_sqG8130_provenance
a
np:Provenance
.
dgn-np:NP806069.RAWYjCyzmzNzZkhnrJ9dBxpGAI3V9lDROB112UJo_sqG8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP806069.RAWYjCyzmzNzZkhnrJ9dBxpGAI3V9lDROB112UJo_sqG8130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0038454
a
ncit:C7057
.
dgn-gda:DGNce6dd51b9abcd2a8554fa1aabebef51e
sio:SIO_000628
miriam-gene:4397
,
lld:C0038454
;
a
sio:SIO_001121
.
}
dgn-np:NP806069.RAWYjCyzmzNzZkhnrJ9dBxpGAI3V9lDROB112UJo_sqG8130_provenance
{
dgn-np:NP806069.RAWYjCyzmzNzZkhnrJ9dBxpGAI3V9lDROB112UJo_sqG8130_assertion
dcterms:description
"[In addition, in models of conditions like stroke, periventricular leukomalacia leading to cerebral palsy, spinal cord injury and multiple sclerosis, oligodendrocytes are damaged by glutamate and, contrary to dogma, it has recently been discovered that this damage is mediated in part by N-methyl-D-aspartate receptors.]. 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:17049173
;
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:NP806069.RAWYjCyzmzNzZkhnrJ9dBxpGAI3V9lDROB112UJo_sqG8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:14+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" .
}