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http://rdf.disgenet.org/nanopublications.trig#NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk
> .
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http://www.w3.org/2000/01/rdf-schema#
> .
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http://www.w3.org/2001/XMLSchema#
> .
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http://semanticscience.org/resource/
> .
@prefix ncit: <
http://ncicb.nci.nih.gov/xml/owl/EVS/Thesaurus.owl#
> .
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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#
> .
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http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
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{
this:
np:hasAssertion
dgn-np:NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_assertion
a
np:Assertion
.
dgn-np:NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_provenance
a
np:Provenance
.
dgn-np:NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_publicationInfo
a
np:PublicationInfo
.
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{
miriam-gene:85358
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNdc45c4a1ea8f5363f487b27fa9455498
sio:SIO_000628
miriam-gene:85358
,
lld:C0004352
;
a
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.
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dgn-np:NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_provenance
{
dgn-np:NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_assertion
dcterms:description
"[To further analyse the involvement of SHANK3 in ASD, we screened the International Molecular Genetic Study of Autism Consortium (IMGSAC) multiplex family sample, 330 families, for SNP association and copy number variants (CNVs) in SHANK3.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:19384346
;
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 .
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dgn-np:NP399562.RAZWTXAdk5PU4J756oxj_shP1UGkA_woZSpcEe3NZnPuk130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
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pav:authoredBy
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> , <
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http://orcid.org/0000-0002-9383-528X
> , <
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> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
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