@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP928239.RAChln2DiZ2Rtcul8Kk7QE6fUw2wK22AlIgmeTUP3_KGE
> .
@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:NP928239.RAChln2DiZ2Rtcul8Kk7QE6fUw2wK22AlIgmeTUP3_KGE130_head
{
this:
np:hasAssertion
dgn-np:NP928239.RAChln2DiZ2Rtcul8Kk7QE6fUw2wK22AlIgmeTUP3_KGE130_assertion
;
np:hasProvenance
dgn-np:NP928239.RAChln2DiZ2Rtcul8Kk7QE6fUw2wK22AlIgmeTUP3_KGE130_provenance
;
np:hasPublicationInfo
dgn-np:NP928239.RAChln2DiZ2Rtcul8Kk7QE6fUw2wK22AlIgmeTUP3_KGE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP928239.RAChln2DiZ2Rtcul8Kk7QE6fUw2wK22AlIgmeTUP3_KGE130_assertion
a
np:Assertion
.
dgn-np:NP928239.RAChln2DiZ2Rtcul8Kk7QE6fUw2wK22AlIgmeTUP3_KGE130_provenance
a
np:Provenance
.
dgn-np:NP928239.RAChln2DiZ2Rtcul8Kk7QE6fUw2wK22AlIgmeTUP3_KGE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP928239.RAChln2DiZ2Rtcul8Kk7QE6fUw2wK22AlIgmeTUP3_KGE130_assertion
{
miriam-gene:3092
a
ncit:C16612
.
lld:C0036572
a
ncit:C7057
.
dgn-gda:DGN8cadc140ed1e0993eb0badf94ff58943
sio:SIO_000628
miriam-gene:3092
,
lld:C0036572
;
a
sio:SIO_001121
.
}
dgn-np:NP928239.RAChln2DiZ2Rtcul8Kk7QE6fUw2wK22AlIgmeTUP3_KGE130_provenance
{
dgn-np:NP928239.RAChln2DiZ2Rtcul8Kk7QE6fUw2wK22AlIgmeTUP3_KGE130_assertion
dcterms:description
"[Based on the current knowledge of Hip1 protein function and its proposed role in AMPA and NMDA ionotropic glutamate receptor trafficking, we believe that HIP1 haploinsufficiency in humans will be amenable to rational drug design for improved seizure control and cognitive and behavioral function.]. 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:21109226
;
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:NP928239.RAChln2DiZ2Rtcul8Kk7QE6fUw2wK22AlIgmeTUP3_KGE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:29+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" .
}