@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss
> .
@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:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_assertion
;
np:hasProvenance
dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_provenance
;
np:hasPublicationInfo
dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_assertion
a
np:Assertion
.
dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_provenance
a
np:Provenance
.
dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_assertion
{
miriam-gene:9289
a
ncit:C16612
.
lld:C0001614
a
ncit:C7057
.
dgn-gda:DGNda7ac865df1beafdcfa296dbf90e4074
sio:SIO_000628
miriam-gene:9289
,
lld:C0001614
;
a
sio:SIO_001121
.
}
dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_provenance
{
dgn-np:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_assertion
dcterms:description
"[Functional studies of the GPR56 gene product will yield insights not only into the causes of polymicrogyria but also into the mechanisms of normal cortical development and the regional patterning of the cerebral cortex.]. 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:15863665
;
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:NP253971.RAgLSld_qYprAuFbBWEeR9HagcgyJDXw0WpI5FDacQlss130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:22+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
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"v2.1.0" .
}