@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP193257.RAcDpqaQ6O8dDWuEdkqvr2Vut4gKoGw8Oniz4mC7UrElo
> .
@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:NP193257.RAcDpqaQ6O8dDWuEdkqvr2Vut4gKoGw8Oniz4mC7UrElo130_head
{
this:
np:hasAssertion
dgn-np:NP193257.RAcDpqaQ6O8dDWuEdkqvr2Vut4gKoGw8Oniz4mC7UrElo130_assertion
;
np:hasProvenance
dgn-np:NP193257.RAcDpqaQ6O8dDWuEdkqvr2Vut4gKoGw8Oniz4mC7UrElo130_provenance
;
np:hasPublicationInfo
dgn-np:NP193257.RAcDpqaQ6O8dDWuEdkqvr2Vut4gKoGw8Oniz4mC7UrElo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP193257.RAcDpqaQ6O8dDWuEdkqvr2Vut4gKoGw8Oniz4mC7UrElo130_assertion
a
np:Assertion
.
dgn-np:NP193257.RAcDpqaQ6O8dDWuEdkqvr2Vut4gKoGw8Oniz4mC7UrElo130_provenance
a
np:Provenance
.
dgn-np:NP193257.RAcDpqaQ6O8dDWuEdkqvr2Vut4gKoGw8Oniz4mC7UrElo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP193257.RAcDpqaQ6O8dDWuEdkqvr2Vut4gKoGw8Oniz4mC7UrElo130_assertion
{
miriam-gene:22871
a
ncit:C16612
.
lld:C0004352
a
ncit:C7057
.
dgn-gda:DGN552a74ae836d98e0359003a9ced1d4ee
sio:SIO_000628
miriam-gene:22871
,
lld:C0004352
;
a
sio:SIO_001121
.
}
dgn-np:NP193257.RAcDpqaQ6O8dDWuEdkqvr2Vut4gKoGw8Oniz4mC7UrElo130_provenance
{
dgn-np:NP193257.RAcDpqaQ6O8dDWuEdkqvr2Vut4gKoGw8Oniz4mC7UrElo130_assertion
dcterms:description
"[The neuroligin gene family consists of five members (NLGN1 at 3q26, NLGN2 at 17p13, NLGN3 at Xq13, NLGN4 at Xp22, and NLGN4Y at Yq11), of which NLGN1 and NLGN3 are located within the best loci observed in our previous genome-wide scan for autism in the Finnish sample.]. 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:16077734
;
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:NP193257.RAcDpqaQ6O8dDWuEdkqvr2Vut4gKoGw8Oniz4mC7UrElo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:46+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" .
}