@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o
> .
@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:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_head
{
this:
np:hasAssertion
dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_assertion
;
np:hasProvenance
dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_provenance
;
np:hasPublicationInfo
dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_assertion
a
np:Assertion
.
dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_provenance
a
np:Provenance
.
dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_assertion
{
miriam-gene:3251
a
ncit:C16612
.
lld:C0000768
a
ncit:C7057
.
dgn-gda:DGN1def347b2c9740c47a189fc032baa916
sio:SIO_000628
miriam-gene:3251
,
lld:C0000768
;
a
sio:SIO_001121
.
}
dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_provenance
{
dgn-np:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_assertion
dcterms:description
"[These demonstrations of dysregulated Wnt signaling and presenilin-1 expression together with impaired expression of dopaminergic transcription factors reveal broad pleitropic neuro-regulatory defects played by HPRT expression and suggest new directions for investigating mechanisms of aberrant neurogenesis and neuropathology in LND and potential new targets for restoration of effective signaling in this neuro-developmental defect.]. 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:21305049
;
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:NP165788.RAA7ceGV7ztlUpnb5lb-QP5Wo6Hi_PaYMxRj1JPTF1m_o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:29+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" .
}