@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE
> .
@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:NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_head
{
this:
np:hasAssertion
dgn-np:NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_assertion
;
np:hasProvenance
dgn-np:NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_provenance
;
np:hasPublicationInfo
dgn-np:NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_assertion
a
np:Assertion
.
dgn-np:NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_provenance
a
np:Provenance
.
dgn-np:NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_assertion
{
miriam-gene:57502
a
ncit:C16612
.
lld:C1510586
a
ncit:C7057
.
dgn-gda:DGNfb957033ce36499734057269dd655ad4
sio:SIO_000628
miriam-gene:57502
,
lld:C1510586
;
a
sio:SIO_001121
.
}
dgn-np:NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_provenance
{
dgn-np:NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_assertion
dcterms:description
"[Synaptic genes, NLGN3 and NLGN4X, two homologous members of the neuroligin family, have been supposed as predisposition loci for autism spectrum disorders (ASDs), and defects of these two genes have been identified in a small fraction of individuals with ASDs.]. 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:21569590
;
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:NP615370.RAlAbw4KVVFaVioZs4dQDQ0QCUQqcfU_-xSHeX7npdWcE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:12+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" .
}