@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP866228.RA9x3gw_CqcrV1N6bNMc3phZzSbbj1VDpxGVl-oKzMuUY
> .
@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:NP866228.RA9x3gw_CqcrV1N6bNMc3phZzSbbj1VDpxGVl-oKzMuUY130_head
{
this:
np:hasAssertion
dgn-np:NP866228.RA9x3gw_CqcrV1N6bNMc3phZzSbbj1VDpxGVl-oKzMuUY130_assertion
;
np:hasProvenance
dgn-np:NP866228.RA9x3gw_CqcrV1N6bNMc3phZzSbbj1VDpxGVl-oKzMuUY130_provenance
;
np:hasPublicationInfo
dgn-np:NP866228.RA9x3gw_CqcrV1N6bNMc3phZzSbbj1VDpxGVl-oKzMuUY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP866228.RA9x3gw_CqcrV1N6bNMc3phZzSbbj1VDpxGVl-oKzMuUY130_assertion
a
np:Assertion
.
dgn-np:NP866228.RA9x3gw_CqcrV1N6bNMc3phZzSbbj1VDpxGVl-oKzMuUY130_provenance
a
np:Provenance
.
dgn-np:NP866228.RA9x3gw_CqcrV1N6bNMc3phZzSbbj1VDpxGVl-oKzMuUY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP866228.RA9x3gw_CqcrV1N6bNMc3phZzSbbj1VDpxGVl-oKzMuUY130_assertion
{
miriam-gene:22941
a
ncit:C16612
.
lld:C0018817
a
ncit:C7057
.
dgn-gda:DGN24b1329427aeb4a04c3f91f0bbbc6ede
sio:SIO_000628
miriam-gene:22941
,
lld:C0018817
;
a
sio:SIO_001121
.
}
dgn-np:NP866228.RA9x3gw_CqcrV1N6bNMc3phZzSbbj1VDpxGVl-oKzMuUY130_provenance
{
dgn-np:NP866228.RA9x3gw_CqcrV1N6bNMc3phZzSbbj1VDpxGVl-oKzMuUY130_assertion
dcterms:description
"[Deficiency of SHANK family genes causing ASD represent an exciting opportunity for developing molecular therapies because of strong genetic evidence for SHANK as causative genes in ASD and the availability of a panel of Shank mutant mouse models.]. 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:23536326
;
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:NP866228.RA9x3gw_CqcrV1N6bNMc3phZzSbbj1VDpxGVl-oKzMuUY130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:27+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" .
}