@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP167671.RAPExBcypCSfIpaLLHBtOrP3g4loibjgupuCmOwlRvbQc
> .
@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:NP167671.RAPExBcypCSfIpaLLHBtOrP3g4loibjgupuCmOwlRvbQc130_head
{
this:
np:hasAssertion
dgn-np:NP167671.RAPExBcypCSfIpaLLHBtOrP3g4loibjgupuCmOwlRvbQc130_assertion
;
np:hasProvenance
dgn-np:NP167671.RAPExBcypCSfIpaLLHBtOrP3g4loibjgupuCmOwlRvbQc130_provenance
;
np:hasPublicationInfo
dgn-np:NP167671.RAPExBcypCSfIpaLLHBtOrP3g4loibjgupuCmOwlRvbQc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP167671.RAPExBcypCSfIpaLLHBtOrP3g4loibjgupuCmOwlRvbQc130_assertion
a
np:Assertion
.
dgn-np:NP167671.RAPExBcypCSfIpaLLHBtOrP3g4loibjgupuCmOwlRvbQc130_provenance
a
np:Provenance
.
dgn-np:NP167671.RAPExBcypCSfIpaLLHBtOrP3g4loibjgupuCmOwlRvbQc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP167671.RAPExBcypCSfIpaLLHBtOrP3g4loibjgupuCmOwlRvbQc130_assertion
{
miriam-gene:57502
a
ncit:C16612
.
lld:C0025362
a
ncit:C7057
.
dgn-gda:DGN6a39d2ebb4a2af19e8524f1e55f3eb19
sio:SIO_000628
miriam-gene:57502
,
lld:C0025362
;
a
sio:SIO_001121
.
}
dgn-np:NP167671.RAPExBcypCSfIpaLLHBtOrP3g4loibjgupuCmOwlRvbQc130_provenance
{
dgn-np:NP167671.RAPExBcypCSfIpaLLHBtOrP3g4loibjgupuCmOwlRvbQc130_assertion
dcterms:description
"[Mutations in neurexin 1 (NRXN1) as well as two other members of the neuroligin family, NLGN3 and NLGN4, have been associated with autism and mutations in NLGN4 have also been associated with intellectual disability, seizures, and EEG abnormalities.]. 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:22106001
;
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:NP167671.RAPExBcypCSfIpaLLHBtOrP3g4loibjgupuCmOwlRvbQc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:30+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" .
}