@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP317136.RASL4oCv3g9bdvdDquYUgt-AFfA-IzJlBqIotftcqeYBU
> .
@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:NP317136.RASL4oCv3g9bdvdDquYUgt-AFfA-IzJlBqIotftcqeYBU130_head
{
this:
np:hasAssertion
dgn-np:NP317136.RASL4oCv3g9bdvdDquYUgt-AFfA-IzJlBqIotftcqeYBU130_assertion
;
np:hasProvenance
dgn-np:NP317136.RASL4oCv3g9bdvdDquYUgt-AFfA-IzJlBqIotftcqeYBU130_provenance
;
np:hasPublicationInfo
dgn-np:NP317136.RASL4oCv3g9bdvdDquYUgt-AFfA-IzJlBqIotftcqeYBU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP317136.RASL4oCv3g9bdvdDquYUgt-AFfA-IzJlBqIotftcqeYBU130_assertion
a
np:Assertion
.
dgn-np:NP317136.RASL4oCv3g9bdvdDquYUgt-AFfA-IzJlBqIotftcqeYBU130_provenance
a
np:Provenance
.
dgn-np:NP317136.RASL4oCv3g9bdvdDquYUgt-AFfA-IzJlBqIotftcqeYBU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP317136.RASL4oCv3g9bdvdDquYUgt-AFfA-IzJlBqIotftcqeYBU130_assertion
{
miriam-gene:3613
a
ncit:C16612
.
lld:C0036341
a
ncit:C7057
.
dgn-gda:DGN10b93c873a726c95155f03ce06dec3b8
sio:SIO_000628
miriam-gene:3613
,
lld:C0036341
;
a
sio:SIO_001121
.
}
dgn-np:NP317136.RASL4oCv3g9bdvdDquYUgt-AFfA-IzJlBqIotftcqeYBU130_provenance
{
dgn-np:NP317136.RASL4oCv3g9bdvdDquYUgt-AFfA-IzJlBqIotftcqeYBU130_assertion
dcterms:description
"[These findings increase the relevance of 18p11.2 to schizophrenia susceptibility because GNAL, which has been shown previously to be implicated in schizophrenia in an independent study, is in close physical proximity to IMPA2.]. 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:11317223
;
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:NP317136.RASL4oCv3g9bdvdDquYUgt-AFfA-IzJlBqIotftcqeYBU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:04+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" .
}