@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP336909.RARDW3eIcLeNW_gYeq3UYeFBW5k09iSzs-XWSnLz2qF0w
> .
@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:NP336909.RARDW3eIcLeNW_gYeq3UYeFBW5k09iSzs-XWSnLz2qF0w130_head
{
this:
np:hasAssertion
dgn-np:NP336909.RARDW3eIcLeNW_gYeq3UYeFBW5k09iSzs-XWSnLz2qF0w130_assertion
;
np:hasProvenance
dgn-np:NP336909.RARDW3eIcLeNW_gYeq3UYeFBW5k09iSzs-XWSnLz2qF0w130_provenance
;
np:hasPublicationInfo
dgn-np:NP336909.RARDW3eIcLeNW_gYeq3UYeFBW5k09iSzs-XWSnLz2qF0w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP336909.RARDW3eIcLeNW_gYeq3UYeFBW5k09iSzs-XWSnLz2qF0w130_assertion
a
np:Assertion
.
dgn-np:NP336909.RARDW3eIcLeNW_gYeq3UYeFBW5k09iSzs-XWSnLz2qF0w130_provenance
a
np:Provenance
.
dgn-np:NP336909.RARDW3eIcLeNW_gYeq3UYeFBW5k09iSzs-XWSnLz2qF0w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP336909.RARDW3eIcLeNW_gYeq3UYeFBW5k09iSzs-XWSnLz2qF0w130_assertion
{
miriam-gene:4846
a
ncit:C16612
.
lld:C0524851
a
ncit:C7057
.
dgn-gda:DGN14f47f5f3301a40f4ea9d751b526fc4a
sio:SIO_000628
miriam-gene:4846
,
lld:C0524851
;
a
sio:SIO_001121
.
}
dgn-np:NP336909.RARDW3eIcLeNW_gYeq3UYeFBW5k09iSzs-XWSnLz2qF0w130_provenance
{
dgn-np:NP336909.RARDW3eIcLeNW_gYeq3UYeFBW5k09iSzs-XWSnLz2qF0w130_assertion
dcterms:description
"[Despite the facts that NOS3 is associated with neuritic sprouting, and aberrant neuronal and glial expression of the same molecule has been found in neurodegenerative diseases, it is unlikely that the polymorphism Glu/Asp of the NOS3 gene is involved in the development of LOAD and DLBD.]. 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:14639046
;
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:NP336909.RARDW3eIcLeNW_gYeq3UYeFBW5k09iSzs-XWSnLz2qF0w130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:18+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" .
}