@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP307963.RAuZDZ1MHWZfnwhdCNQsMPXrLFDBqU3beHN1ENVyk2vEw
> .
@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:NP307963.RAuZDZ1MHWZfnwhdCNQsMPXrLFDBqU3beHN1ENVyk2vEw130_head
{
this:
np:hasAssertion
dgn-np:NP307963.RAuZDZ1MHWZfnwhdCNQsMPXrLFDBqU3beHN1ENVyk2vEw130_assertion
;
np:hasProvenance
dgn-np:NP307963.RAuZDZ1MHWZfnwhdCNQsMPXrLFDBqU3beHN1ENVyk2vEw130_provenance
;
np:hasPublicationInfo
dgn-np:NP307963.RAuZDZ1MHWZfnwhdCNQsMPXrLFDBqU3beHN1ENVyk2vEw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP307963.RAuZDZ1MHWZfnwhdCNQsMPXrLFDBqU3beHN1ENVyk2vEw130_assertion
a
np:Assertion
.
dgn-np:NP307963.RAuZDZ1MHWZfnwhdCNQsMPXrLFDBqU3beHN1ENVyk2vEw130_provenance
a
np:Provenance
.
dgn-np:NP307963.RAuZDZ1MHWZfnwhdCNQsMPXrLFDBqU3beHN1ENVyk2vEw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP307963.RAuZDZ1MHWZfnwhdCNQsMPXrLFDBqU3beHN1ENVyk2vEw130_assertion
{
miriam-gene:9378
a
ncit:C16612
.
lld:C0028043
a
ncit:C7057
.
dgn-gda:DGN9e35f4887d1501167202f36503847abc
sio:SIO_000628
miriam-gene:9378
,
lld:C0028043
;
a
sio:SIO_001121
.
}
dgn-np:NP307963.RAuZDZ1MHWZfnwhdCNQsMPXrLFDBqU3beHN1ENVyk2vEw130_provenance
{
dgn-np:NP307963.RAuZDZ1MHWZfnwhdCNQsMPXrLFDBqU3beHN1ENVyk2vEw130_assertion
dcterms:description
"[Based on our findings that NRXN1 has significant association with ND in two independent samples, recent findings that NRXN1 plays an important role in synaptic development, and the previous report of association, we conclude that this gene represents a strong candidate for involvement in the etiology of ND.]. 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:18270208
;
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:NP307963.RAuZDZ1MHWZfnwhdCNQsMPXrLFDBqU3beHN1ENVyk2vEw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:56+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" .
}