@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP960892.RAt2IMaHB4glAEEypo12bX1R74invREfyz1uV8up7G9t8
> .
@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/v3.0.0/void/
> .
dgn-np:NP960892.RAt2IMaHB4glAEEypo12bX1R74invREfyz1uV8up7G9t8130_head
{
this:
np:hasAssertion
dgn-np:NP960892.RAt2IMaHB4glAEEypo12bX1R74invREfyz1uV8up7G9t8130_assertion
;
np:hasProvenance
dgn-np:NP960892.RAt2IMaHB4glAEEypo12bX1R74invREfyz1uV8up7G9t8130_provenance
;
np:hasPublicationInfo
dgn-np:NP960892.RAt2IMaHB4glAEEypo12bX1R74invREfyz1uV8up7G9t8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP960892.RAt2IMaHB4glAEEypo12bX1R74invREfyz1uV8up7G9t8130_assertion
a
np:Assertion
.
dgn-np:NP960892.RAt2IMaHB4glAEEypo12bX1R74invREfyz1uV8up7G9t8130_provenance
a
np:Provenance
.
dgn-np:NP960892.RAt2IMaHB4glAEEypo12bX1R74invREfyz1uV8up7G9t8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP960892.RAt2IMaHB4glAEEypo12bX1R74invREfyz1uV8up7G9t8130_assertion
{
miriam-gene:91752
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNc3cadf72a0b67663004cd7699ad4e3d6
sio:SIO_000628
miriam-gene:91752
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP960892.RAt2IMaHB4glAEEypo12bX1R74invREfyz1uV8up7G9t8130_provenance
{
dgn-np:NP960892.RAt2IMaHB4glAEEypo12bX1R74invREfyz1uV8up7G9t8130_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-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP960892.RAt2IMaHB4glAEEypo12bX1R74invREfyz1uV8up7G9t8130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:47:27+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}