@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1042959.RANUT870_dahbQK4FNeLe8KgqEro5XK0Cnne400C3j56g
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP1042959.RANUT870_dahbQK4FNeLe8KgqEro5XK0Cnne400C3j56g130_assertion
;
np:hasProvenance
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;
np:hasPublicationInfo
dgn-np:NP1042959.RANUT870_dahbQK4FNeLe8KgqEro5XK0Cnne400C3j56g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1042959.RANUT870_dahbQK4FNeLe8KgqEro5XK0Cnne400C3j56g130_assertion
a
np:Assertion
.
dgn-np:NP1042959.RANUT870_dahbQK4FNeLe8KgqEro5XK0Cnne400C3j56g130_provenance
a
np:Provenance
.
dgn-np:NP1042959.RANUT870_dahbQK4FNeLe8KgqEro5XK0Cnne400C3j56g130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:820
a
ncit:C16612
.
lld:C0338656
a
ncit:C7057
.
dgn-gda:DGNae625a673fcf56e3dae9a5a59252e5b2
sio:SIO_000628
miriam-gene:820
,
lld:C0338656
;
a
sio:SIO_001121
.
}
dgn-np:NP1042959.RANUT870_dahbQK4FNeLe8KgqEro5XK0Cnne400C3j56g130_provenance
{
dgn-np:NP1042959.RANUT870_dahbQK4FNeLe8KgqEro5XK0Cnne400C3j56g130_assertion
dcterms:description
"[Further, we describe discoveries from these models that have uncovered defects in the regulation of Ras activity, cAMP generation, and dopamine homeostasis as key mechanisms important for cognitive dysfunction in children with NF1.]. 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:23312374
;
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:NP1042959.RANUT870_dahbQK4FNeLe8KgqEro5XK0Cnne400C3j56g130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:39+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
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;
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" .
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"v4.0.0" .
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