@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP810501.RARyMya-rNejT3pXlxv37AAyFa-vDwcatz3spIkHn0NWA
> .
@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:NP810501.RARyMya-rNejT3pXlxv37AAyFa-vDwcatz3spIkHn0NWA130_head
{
this:
np:hasAssertion
dgn-np:NP810501.RARyMya-rNejT3pXlxv37AAyFa-vDwcatz3spIkHn0NWA130_assertion
;
np:hasProvenance
dgn-np:NP810501.RARyMya-rNejT3pXlxv37AAyFa-vDwcatz3spIkHn0NWA130_provenance
;
np:hasPublicationInfo
dgn-np:NP810501.RARyMya-rNejT3pXlxv37AAyFa-vDwcatz3spIkHn0NWA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP810501.RARyMya-rNejT3pXlxv37AAyFa-vDwcatz3spIkHn0NWA130_assertion
a
np:Assertion
.
dgn-np:NP810501.RARyMya-rNejT3pXlxv37AAyFa-vDwcatz3spIkHn0NWA130_provenance
a
np:Provenance
.
dgn-np:NP810501.RARyMya-rNejT3pXlxv37AAyFa-vDwcatz3spIkHn0NWA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP810501.RARyMya-rNejT3pXlxv37AAyFa-vDwcatz3spIkHn0NWA130_assertion
{
miriam-gene:1006
a
ncit:C16612
.
lld:C1510586
a
ncit:C7057
.
dgn-gda:DGN9dfc081a8f236f9af707698b33eecf25
sio:SIO_000628
miriam-gene:1006
,
lld:C1510586
;
a
sio:SIO_001121
.
}
dgn-np:NP810501.RARyMya-rNejT3pXlxv37AAyFa-vDwcatz3spIkHn0NWA130_provenance
{
dgn-np:NP810501.RARyMya-rNejT3pXlxv37AAyFa-vDwcatz3spIkHn0NWA130_assertion
dcterms:description
"[Examples of such intergenic CNV regions include 16q21 and 2p16.3 near known ASD risk genes CDH8 and NRXN1 respectively, as well as novel loci contiguous with ZHX2, MOCS1, LRRC4C, SEMA3C, and other genes.]. 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:23879678
;
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:NP810501.RARyMya-rNejT3pXlxv37AAyFa-vDwcatz3spIkHn0NWA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:17+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" .
}