@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP325811.RA_OZtnaO_tvr65H8iUsZEmntsDEcweflIlcNQQpifau4
> .
@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:NP325811.RA_OZtnaO_tvr65H8iUsZEmntsDEcweflIlcNQQpifau4130_head
{
this:
np:hasAssertion
dgn-np:NP325811.RA_OZtnaO_tvr65H8iUsZEmntsDEcweflIlcNQQpifau4130_assertion
;
np:hasProvenance
dgn-np:NP325811.RA_OZtnaO_tvr65H8iUsZEmntsDEcweflIlcNQQpifau4130_provenance
;
np:hasPublicationInfo
dgn-np:NP325811.RA_OZtnaO_tvr65H8iUsZEmntsDEcweflIlcNQQpifau4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP325811.RA_OZtnaO_tvr65H8iUsZEmntsDEcweflIlcNQQpifau4130_assertion
a
np:Assertion
.
dgn-np:NP325811.RA_OZtnaO_tvr65H8iUsZEmntsDEcweflIlcNQQpifau4130_provenance
a
np:Provenance
.
dgn-np:NP325811.RA_OZtnaO_tvr65H8iUsZEmntsDEcweflIlcNQQpifau4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP325811.RA_OZtnaO_tvr65H8iUsZEmntsDEcweflIlcNQQpifau4130_assertion
{
miriam-gene:4853
a
ncit:C16612
.
lld:C0271097
a
ncit:C7057
.
dgn-gda:DGN3891dd588f6dfa8a9593e5d3a42fc2f4
sio:SIO_000628
miriam-gene:4853
,
lld:C0271097
;
a
sio:SIO_001121
.
}
dgn-np:NP325811.RA_OZtnaO_tvr65H8iUsZEmntsDEcweflIlcNQQpifau4130_provenance
{
dgn-np:NP325811.RA_OZtnaO_tvr65H8iUsZEmntsDEcweflIlcNQQpifau4130_assertion
dcterms:description
"[Several of the top candidate genes include EEF1A1, ROBO1, PLXNA4, SLIT3, NRP1, and NOTCH2, as well as genes associated with the Usher syndrome, PCDH15 and USH2A, and are plausible candidates contributing to the developmental defects in Gbx2(-/-) mice.]. 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:23144817
;
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:NP325811.RA_OZtnaO_tvr65H8iUsZEmntsDEcweflIlcNQQpifau4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:10+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" .
}