@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_head
{
this:
np:hasAssertion
dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_assertion
;
np:hasProvenance
dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_provenance
;
np:hasPublicationInfo
dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_assertion
a
np:Assertion
.
dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_provenance
a
np:Provenance
.
dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_assertion
{
miriam-gene:3064
a
ncit:C16612
.
lld:C0020179
a
ncit:C7057
.
dgn-gda:DGNde0ff7f1d3e44b65d849c37bd202bce9
sio:SIO_000628
miriam-gene:3064
,
lld:C0020179
;
a
sio:SIO_001121
.
}
dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_provenance
{
dgn-np:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_assertion
dcterms:description
"[HIP14 is dysfunctional in the presence of mutant HTT (mHTT), the causative gene for Huntington disease (HD), and we hypothesize that reduced palmitoylation of HTT and other HIP14 substrates contributes to the pathogenesis of the disease.]. 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:24705354
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP445333.RA03azhBHXIPSynfzMby1wHatceoMbkZWG1kEJjieP-Mk130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:42:00+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}