@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP564109.RA-6AavK7HVB24CwrbpOVPMX5WfEuOH5Cibjtwdbu5DWU
> .
@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:NP564109.RA-6AavK7HVB24CwrbpOVPMX5WfEuOH5Cibjtwdbu5DWU130_head
{
this:
np:hasAssertion
dgn-np:NP564109.RA-6AavK7HVB24CwrbpOVPMX5WfEuOH5Cibjtwdbu5DWU130_assertion
;
np:hasProvenance
dgn-np:NP564109.RA-6AavK7HVB24CwrbpOVPMX5WfEuOH5Cibjtwdbu5DWU130_provenance
;
np:hasPublicationInfo
dgn-np:NP564109.RA-6AavK7HVB24CwrbpOVPMX5WfEuOH5Cibjtwdbu5DWU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP564109.RA-6AavK7HVB24CwrbpOVPMX5WfEuOH5Cibjtwdbu5DWU130_assertion
a
np:Assertion
.
dgn-np:NP564109.RA-6AavK7HVB24CwrbpOVPMX5WfEuOH5Cibjtwdbu5DWU130_provenance
a
np:Provenance
.
dgn-np:NP564109.RA-6AavK7HVB24CwrbpOVPMX5WfEuOH5Cibjtwdbu5DWU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP564109.RA-6AavK7HVB24CwrbpOVPMX5WfEuOH5Cibjtwdbu5DWU130_assertion
{
miriam-gene:5747
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGN3083212ce2254792a3a4e414f086615e
sio:SIO_000628
miriam-gene:5747
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP564109.RA-6AavK7HVB24CwrbpOVPMX5WfEuOH5Cibjtwdbu5DWU130_provenance
{
dgn-np:NP564109.RA-6AavK7HVB24CwrbpOVPMX5WfEuOH5Cibjtwdbu5DWU130_assertion
dcterms:description
"[We suggest that THOC2 can play specific roles in neuronal cells and, possibly in combination with PTK2 reduction, may affect normal neural network formation, leading to cognitive impairment and cerebellar congenital hypoplasia.]. 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:23749989
;
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:NP564109.RA-6AavK7HVB24CwrbpOVPMX5WfEuOH5Cibjtwdbu5DWU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}