@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP134569.RAiWzMZ9AmbQ5wyv3EIasrW0clc3Xnbrv3K0OwZznxFw0
> .
@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:NP134569.RAiWzMZ9AmbQ5wyv3EIasrW0clc3Xnbrv3K0OwZznxFw0130_head
{
this:
np:hasAssertion
dgn-np:NP134569.RAiWzMZ9AmbQ5wyv3EIasrW0clc3Xnbrv3K0OwZznxFw0130_assertion
;
np:hasProvenance
dgn-np:NP134569.RAiWzMZ9AmbQ5wyv3EIasrW0clc3Xnbrv3K0OwZznxFw0130_provenance
;
np:hasPublicationInfo
dgn-np:NP134569.RAiWzMZ9AmbQ5wyv3EIasrW0clc3Xnbrv3K0OwZznxFw0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP134569.RAiWzMZ9AmbQ5wyv3EIasrW0clc3Xnbrv3K0OwZznxFw0130_assertion
a
np:Assertion
.
dgn-np:NP134569.RAiWzMZ9AmbQ5wyv3EIasrW0clc3Xnbrv3K0OwZznxFw0130_provenance
a
np:Provenance
.
dgn-np:NP134569.RAiWzMZ9AmbQ5wyv3EIasrW0clc3Xnbrv3K0OwZznxFw0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP134569.RAiWzMZ9AmbQ5wyv3EIasrW0clc3Xnbrv3K0OwZznxFw0130_assertion
{
miriam-gene:22829
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGNf3de1dd4049c11cacefe789e36dfe8c0
sio:SIO_000628
miriam-gene:22829
,
lld:C0004352
;
a
sio:SIO_001122
.
}
dgn-np:NP134569.RAiWzMZ9AmbQ5wyv3EIasrW0clc3Xnbrv3K0OwZznxFw0130_provenance
{
dgn-np:NP134569.RAiWzMZ9AmbQ5wyv3EIasrW0clc3Xnbrv3K0OwZznxFw0130_assertion
dcterms:description
"[The coding sequences and splice junctions of the NLGN4Y gene were analyzed in 335 male samples (290 with autism and 45 with mental retardation) to analyze sequence variants in NLGN4Y that are associated with autism or mental retardation.]. 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:18628683
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP134569.RAiWzMZ9AmbQ5wyv3EIasrW0clc3Xnbrv3K0OwZznxFw0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:10+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" .
}