@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP417014.RAiRUGmfle8EwGOiwes4OOopx2ZkeXh_kFSNC09l-DilA
> .
@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:NP417014.RAiRUGmfle8EwGOiwes4OOopx2ZkeXh_kFSNC09l-DilA130_head
{
this:
np:hasAssertion
dgn-np:NP417014.RAiRUGmfle8EwGOiwes4OOopx2ZkeXh_kFSNC09l-DilA130_assertion
;
np:hasProvenance
dgn-np:NP417014.RAiRUGmfle8EwGOiwes4OOopx2ZkeXh_kFSNC09l-DilA130_provenance
;
np:hasPublicationInfo
dgn-np:NP417014.RAiRUGmfle8EwGOiwes4OOopx2ZkeXh_kFSNC09l-DilA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP417014.RAiRUGmfle8EwGOiwes4OOopx2ZkeXh_kFSNC09l-DilA130_assertion
a
np:Assertion
.
dgn-np:NP417014.RAiRUGmfle8EwGOiwes4OOopx2ZkeXh_kFSNC09l-DilA130_provenance
a
np:Provenance
.
dgn-np:NP417014.RAiRUGmfle8EwGOiwes4OOopx2ZkeXh_kFSNC09l-DilA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP417014.RAiRUGmfle8EwGOiwes4OOopx2ZkeXh_kFSNC09l-DilA130_assertion
{
miriam-gene:2562
a
ncit:C16612
.
lld:C0162635
a
ncit:C7057
.
dgn-gda:DGNff69bb8216967f7a68eb912ea1cc6a75
sio:SIO_000628
miriam-gene:2562
,
lld:C0162635
;
a
sio:SIO_001121
.
}
dgn-np:NP417014.RAiRUGmfle8EwGOiwes4OOopx2ZkeXh_kFSNC09l-DilA130_provenance
{
dgn-np:NP417014.RAiRUGmfle8EwGOiwes4OOopx2ZkeXh_kFSNC09l-DilA130_assertion
dcterms:description
"[The loss of the single gene, gabrb3, in these mice is sufficient to cause phenotypic traits that have marked similarities to the clinical features of AS, indicating that impaired expression of the GABRB3 gene in humans probably contributes to the overall phenotype of Angelman syndrome.]. 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:9763493
;
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:NP417014.RAiRUGmfle8EwGOiwes4OOopx2ZkeXh_kFSNC09l-DilA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:41:42+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" .
}