@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM
> .
@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:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_head
{
this:
np:hasAssertion
dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_assertion
;
np:hasProvenance
dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_provenance
;
np:hasPublicationInfo
dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_assertion
a
np:Assertion
.
dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_provenance
a
np:Provenance
.
dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_assertion
{
miriam-gene:3480
a
ncit:C16612
.
lld:C0010278
a
ncit:C7057
.
dgn-gda:DGNe8b4e9976491f785c335ba5bcb61d22c
sio:SIO_000628
miriam-gene:3480
,
lld:C0010278
;
a
sio:SIO_001121
.
}
dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_provenance
{
dgn-np:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_assertion
dcterms:description
"[Taken together, these results suggest that despite the stimulation of different pathways, activating phosphorylation patterns for IRS1 were consistent in cell lines from both subtypes and the IGF1R variants, thus implicating a key role for IRS1 in the pathogenesis of nonsyndromic craniosynostosis.]. 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:23073384
;
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:NP325253.RAT1BFDbBYaV5bgEPDmYNpUpUZkBKq8vlReHYvoLmKoDM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:10+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" .
}