@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP579657.RANt1Sj5PR1OyHy-LJIAUMJYEHef2D_31nMVJSn64dkTU
> .
@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:NP579657.RANt1Sj5PR1OyHy-LJIAUMJYEHef2D_31nMVJSn64dkTU130_head
{
this:
np:hasAssertion
dgn-np:NP579657.RANt1Sj5PR1OyHy-LJIAUMJYEHef2D_31nMVJSn64dkTU130_assertion
;
np:hasProvenance
dgn-np:NP579657.RANt1Sj5PR1OyHy-LJIAUMJYEHef2D_31nMVJSn64dkTU130_provenance
;
np:hasPublicationInfo
dgn-np:NP579657.RANt1Sj5PR1OyHy-LJIAUMJYEHef2D_31nMVJSn64dkTU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP579657.RANt1Sj5PR1OyHy-LJIAUMJYEHef2D_31nMVJSn64dkTU130_assertion
a
np:Assertion
.
dgn-np:NP579657.RANt1Sj5PR1OyHy-LJIAUMJYEHef2D_31nMVJSn64dkTU130_provenance
a
np:Provenance
.
dgn-np:NP579657.RANt1Sj5PR1OyHy-LJIAUMJYEHef2D_31nMVJSn64dkTU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP579657.RANt1Sj5PR1OyHy-LJIAUMJYEHef2D_31nMVJSn64dkTU130_assertion
{
miriam-gene:4397
a
ncit:C16612
.
lld:C0002736
a
ncit:C7057
.
dgn-gda:DGN6bda18f963b44f9fb50f15f1d1c145eb
sio:SIO_000628
miriam-gene:4397
,
lld:C0002736
;
a
sio:SIO_001121
.
}
dgn-np:NP579657.RANt1Sj5PR1OyHy-LJIAUMJYEHef2D_31nMVJSn64dkTU130_provenance
{
dgn-np:NP579657.RANt1Sj5PR1OyHy-LJIAUMJYEHef2D_31nMVJSn64dkTU130_assertion
dcterms:description
"[It can be occur in neurodegenerative disorders, such as Parkinson's disease, Huntington's and Alzheimer's disease, in stroke, in epilepsy, in multiple sclerosis, in amyotrophic lateral sclerosis, and in mental failures, such as schizophrenia and depression.]. 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:17017544
;
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:NP579657.RANt1Sj5PR1OyHy-LJIAUMJYEHef2D_31nMVJSn64dkTU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:49+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" .
}