@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg
> .
@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:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_head
{
this:
np:hasAssertion
dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_assertion
;
np:hasProvenance
dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_provenance
;
np:hasPublicationInfo
dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_assertion
a
np:Assertion
.
dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_provenance
a
np:Provenance
.
dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_assertion
{
miriam-gene:11331
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNd413d79316361ee07c048f9bae9d901d
sio:SIO_000628
miriam-gene:11331
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_provenance
{
dgn-np:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_assertion
dcterms:description
"[Studies of this broad autism phenotype (BAP) may provide a potentially important complementary approach for detecting the genes causing autism and defining associated neural circuitry by identifying more refined phenotypes that can be measured quantitatively in both affected and unaffected individuals and that are tied to functioning in particular regions of the brain.]. 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:19414711
;
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:NP420283.RAGa0YnKkbqeoYv40q-mTI93RYldPN7FASeh4kUbkRIwg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:09+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" .
}