@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP376002.RAgEb6Ich1NW1pCsmcs3JrFoSHG5Arrt8Khb4jO4MgB6A
> .
@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:NP376002.RAgEb6Ich1NW1pCsmcs3JrFoSHG5Arrt8Khb4jO4MgB6A130_head
{
this:
np:hasAssertion
dgn-np:NP376002.RAgEb6Ich1NW1pCsmcs3JrFoSHG5Arrt8Khb4jO4MgB6A130_assertion
;
np:hasProvenance
dgn-np:NP376002.RAgEb6Ich1NW1pCsmcs3JrFoSHG5Arrt8Khb4jO4MgB6A130_provenance
;
np:hasPublicationInfo
dgn-np:NP376002.RAgEb6Ich1NW1pCsmcs3JrFoSHG5Arrt8Khb4jO4MgB6A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP376002.RAgEb6Ich1NW1pCsmcs3JrFoSHG5Arrt8Khb4jO4MgB6A130_assertion
a
np:Assertion
.
dgn-np:NP376002.RAgEb6Ich1NW1pCsmcs3JrFoSHG5Arrt8Khb4jO4MgB6A130_provenance
a
np:Provenance
.
dgn-np:NP376002.RAgEb6Ich1NW1pCsmcs3JrFoSHG5Arrt8Khb4jO4MgB6A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP376002.RAgEb6Ich1NW1pCsmcs3JrFoSHG5Arrt8Khb4jO4MgB6A130_assertion
{
miriam-gene:5663
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN0b454f09f9fa63a260eecb8a0969d763
sio:SIO_000628
miriam-gene:5663
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP376002.RAgEb6Ich1NW1pCsmcs3JrFoSHG5Arrt8Khb4jO4MgB6A130_provenance
{
dgn-np:NP376002.RAgEb6Ich1NW1pCsmcs3JrFoSHG5Arrt8Khb4jO4MgB6A130_assertion
dcterms:description
"[There is new hope that these new avenues will help understanding the neurobiology of schizophrenia in more depth leading to the development of new innovative diagnostic tools and therapies as was the case after the discovery of rare APP and presenilin 1 and 2 mutations in Alzheimer's disease.]. 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:19526738
;
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:NP376002.RAgEb6Ich1NW1pCsmcs3JrFoSHG5Arrt8Khb4jO4MgB6A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:40+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" .
}