@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP729090.RAkZBz9Yj5IzOm62KI0se6pk53p5EFR6vVDYdrRQXwows
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP729090.RAkZBz9Yj5IzOm62KI0se6pk53p5EFR6vVDYdrRQXwows130_head
{
this:
np:hasAssertion
dgn-np:NP729090.RAkZBz9Yj5IzOm62KI0se6pk53p5EFR6vVDYdrRQXwows130_assertion
;
np:hasProvenance
dgn-np:NP729090.RAkZBz9Yj5IzOm62KI0se6pk53p5EFR6vVDYdrRQXwows130_provenance
;
np:hasPublicationInfo
dgn-np:NP729090.RAkZBz9Yj5IzOm62KI0se6pk53p5EFR6vVDYdrRQXwows130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP729090.RAkZBz9Yj5IzOm62KI0se6pk53p5EFR6vVDYdrRQXwows130_assertion
a
np:Assertion
.
dgn-np:NP729090.RAkZBz9Yj5IzOm62KI0se6pk53p5EFR6vVDYdrRQXwows130_provenance
a
np:Provenance
.
dgn-np:NP729090.RAkZBz9Yj5IzOm62KI0se6pk53p5EFR6vVDYdrRQXwows130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP729090.RAkZBz9Yj5IzOm62KI0se6pk53p5EFR6vVDYdrRQXwows130_assertion
{
miriam-gene:91752
a
ncit:C16612
.
lld:C0014544
a
ncit:C7057
.
dgn-gda:DGNca5e295c1b5f12d234dc46d7976ee5f6
sio:SIO_000628
miriam-gene:91752
,
lld:C0014544
;
a
sio:SIO_001121
.
}
dgn-np:NP729090.RAkZBz9Yj5IzOm62KI0se6pk53p5EFR6vVDYdrRQXwows130_provenance
{
dgn-np:NP729090.RAkZBz9Yj5IzOm62KI0se6pk53p5EFR6vVDYdrRQXwows130_assertion
dcterms:description
"[For example, variation at ZNF804A is associated with risk of both bipolar disorder and schizophrenia, and some rare CNVs are associated with risk of autism and epilepsy as well as schizophrenia.]. 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:19329560
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP729090.RAkZBz9Yj5IzOm62KI0se6pk53p5EFR6vVDYdrRQXwows130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:15+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}