@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP903376.RAEeZV3KUEKpNVzQ4CVK_yuy5_1ITQQEAYxFRbWqyqN0Y
> .
@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:NP903376.RAEeZV3KUEKpNVzQ4CVK_yuy5_1ITQQEAYxFRbWqyqN0Y130_head
{
this:
np:hasAssertion
dgn-np:NP903376.RAEeZV3KUEKpNVzQ4CVK_yuy5_1ITQQEAYxFRbWqyqN0Y130_assertion
;
np:hasProvenance
dgn-np:NP903376.RAEeZV3KUEKpNVzQ4CVK_yuy5_1ITQQEAYxFRbWqyqN0Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP903376.RAEeZV3KUEKpNVzQ4CVK_yuy5_1ITQQEAYxFRbWqyqN0Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP903376.RAEeZV3KUEKpNVzQ4CVK_yuy5_1ITQQEAYxFRbWqyqN0Y130_assertion
a
np:Assertion
.
dgn-np:NP903376.RAEeZV3KUEKpNVzQ4CVK_yuy5_1ITQQEAYxFRbWqyqN0Y130_provenance
a
np:Provenance
.
dgn-np:NP903376.RAEeZV3KUEKpNVzQ4CVK_yuy5_1ITQQEAYxFRbWqyqN0Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP903376.RAEeZV3KUEKpNVzQ4CVK_yuy5_1ITQQEAYxFRbWqyqN0Y130_assertion
{
miriam-gene:351
a
ncit:C16612
.
lld:C0221505
a
ncit:C7057
.
dgn-gda:DGN77f88c0de3d36573dd9229f766f014d8
sio:SIO_000628
miriam-gene:351
,
lld:C0221505
;
a
sio:SIO_001121
.
}
dgn-np:NP903376.RAEeZV3KUEKpNVzQ4CVK_yuy5_1ITQQEAYxFRbWqyqN0Y130_provenance
{
dgn-np:NP903376.RAEeZV3KUEKpNVzQ4CVK_yuy5_1ITQQEAYxFRbWqyqN0Y130_assertion
dcterms:description
"[The results of the present study show that expression of both iNOS and eNOS is increased in activated astrocytes under experimental conditions associated with elevated expression of APP (electrolytic brain lesion) or Abeta-deposition (APP23 transgenic mice).]. 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:11532247
;
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:NP903376.RAEeZV3KUEKpNVzQ4CVK_yuy5_1ITQQEAYxFRbWqyqN0Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:15+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" .
}