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http://rdf.disgenet.org/nanopublications.trig#NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_assertion
;
np:hasProvenance
dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_provenance
;
np:hasPublicationInfo
dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_assertion
a
np:Assertion
.
dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_provenance
a
np:Provenance
.
dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_assertion
{
miriam-gene:57556
a
ncit:C16612
.
lld:C0004936
a
ncit:C7057
.
dgn-gda:DGN932efaf588204bfdd18475b0bb985124
sio:SIO_000628
miriam-gene:57556
,
lld:C0004936
;
a
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.
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dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_provenance
{
dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_assertion
dcterms:description
"[Mice with mutations in Sema6A or the interacting genes may thus represent a highly informative model for how neurodevelopmental defects can lead to anatomical dysconnectivity, resulting, either directly or through reactive mechanisms, in dysfunction at the level of neuronal networks with associated behavioural phenotypes of relevance to psychiatric disorders.]. 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:22132072
;
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 .
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dgn-np:NP816414.RAvDUjTsmQou53yCAOb-bvKYdtGAsthrwb2TUIG6xB5Sc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:20+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
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pav:authoredBy
<
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> , <
http://orcid.org/0000-0002-7534-7661
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> , <
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" .
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"v2.1.0" .
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