@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP833880.RAig6pbRbmX39gsLZChtT3IDq4lNeco8dkXIY_3WxMyEo
> .
@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/v4.0.0/void/
> .
dgn-np:NP833880.RAig6pbRbmX39gsLZChtT3IDq4lNeco8dkXIY_3WxMyEo130_head
{
this:
np:hasAssertion
dgn-np:NP833880.RAig6pbRbmX39gsLZChtT3IDq4lNeco8dkXIY_3WxMyEo130_assertion
;
np:hasProvenance
dgn-np:NP833880.RAig6pbRbmX39gsLZChtT3IDq4lNeco8dkXIY_3WxMyEo130_provenance
;
np:hasPublicationInfo
dgn-np:NP833880.RAig6pbRbmX39gsLZChtT3IDq4lNeco8dkXIY_3WxMyEo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP833880.RAig6pbRbmX39gsLZChtT3IDq4lNeco8dkXIY_3WxMyEo130_assertion
a
np:Assertion
.
dgn-np:NP833880.RAig6pbRbmX39gsLZChtT3IDq4lNeco8dkXIY_3WxMyEo130_provenance
a
np:Provenance
.
dgn-np:NP833880.RAig6pbRbmX39gsLZChtT3IDq4lNeco8dkXIY_3WxMyEo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP833880.RAig6pbRbmX39gsLZChtT3IDq4lNeco8dkXIY_3WxMyEo130_assertion
{
miriam-gene:445
a
ncit:C16612
.
lld:C0085584
a
ncit:C7057
.
dgn-gda:DGN3fee6bc145c9d44720231524d6c0c5e8
sio:SIO_000628
miriam-gene:445
,
lld:C0085584
;
a
sio:SIO_001121
.
}
dgn-np:NP833880.RAig6pbRbmX39gsLZChtT3IDq4lNeco8dkXIY_3WxMyEo130_provenance
{
dgn-np:NP833880.RAig6pbRbmX39gsLZChtT3IDq4lNeco8dkXIY_3WxMyEo130_assertion
dcterms:description
"[These mouse mutations constitute a suitable model for both mechanistic and preclinical studies of CTLN1 and other hyperammonemic encephalopathies and, at the same time, underscore the importance of complementing knockout mutations with hypomorphic mutations for the generation of animal models of human genetic diseases.]. 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:20724589
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP833880.RAig6pbRbmX39gsLZChtT3IDq4lNeco8dkXIY_3WxMyEo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:48:02+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}