@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP240513.RAjl5vcUtTj6naGDm6ifBIdyk83JCh9mAY7RPao2KZ0-c
> .
@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:NP240513.RAjl5vcUtTj6naGDm6ifBIdyk83JCh9mAY7RPao2KZ0-c130_head
{
this:
np:hasAssertion
dgn-np:NP240513.RAjl5vcUtTj6naGDm6ifBIdyk83JCh9mAY7RPao2KZ0-c130_assertion
;
np:hasProvenance
dgn-np:NP240513.RAjl5vcUtTj6naGDm6ifBIdyk83JCh9mAY7RPao2KZ0-c130_provenance
;
np:hasPublicationInfo
dgn-np:NP240513.RAjl5vcUtTj6naGDm6ifBIdyk83JCh9mAY7RPao2KZ0-c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP240513.RAjl5vcUtTj6naGDm6ifBIdyk83JCh9mAY7RPao2KZ0-c130_assertion
a
np:Assertion
.
dgn-np:NP240513.RAjl5vcUtTj6naGDm6ifBIdyk83JCh9mAY7RPao2KZ0-c130_provenance
a
np:Provenance
.
dgn-np:NP240513.RAjl5vcUtTj6naGDm6ifBIdyk83JCh9mAY7RPao2KZ0-c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP240513.RAjl5vcUtTj6naGDm6ifBIdyk83JCh9mAY7RPao2KZ0-c130_assertion
{
miriam-gene:57502
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGNdfc42f970b3c4a247c370b6e0a881c8e
sio:SIO_000628
miriam-gene:57502
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP240513.RAjl5vcUtTj6naGDm6ifBIdyk83JCh9mAY7RPao2KZ0-c130_provenance
{
dgn-np:NP240513.RAjl5vcUtTj6naGDm6ifBIdyk83JCh9mAY7RPao2KZ0-c130_assertion
dcterms:description
"[The fact that the deletion was present in both autistic and nonautistic mentally retarded males suggests that the NLGN4 gene is not only involved in autism, as previously described, but also in mental retardation, indicating that some types of autistic disorder and mental retardation may have common genetic origins.]. 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:14963808
;
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:NP240513.RAjl5vcUtTj6naGDm6ifBIdyk83JCh9mAY7RPao2KZ0-c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}