@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP590198.RAsHvA_lJ_KffAARVDR6wZ1kZ8VvadaPqGBya_yw4Z4eQ
> .
@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:NP590198.RAsHvA_lJ_KffAARVDR6wZ1kZ8VvadaPqGBya_yw4Z4eQ130_head
{
this:
np:hasAssertion
dgn-np:NP590198.RAsHvA_lJ_KffAARVDR6wZ1kZ8VvadaPqGBya_yw4Z4eQ130_assertion
;
np:hasProvenance
dgn-np:NP590198.RAsHvA_lJ_KffAARVDR6wZ1kZ8VvadaPqGBya_yw4Z4eQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP590198.RAsHvA_lJ_KffAARVDR6wZ1kZ8VvadaPqGBya_yw4Z4eQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP590198.RAsHvA_lJ_KffAARVDR6wZ1kZ8VvadaPqGBya_yw4Z4eQ130_assertion
a
np:Assertion
.
dgn-np:NP590198.RAsHvA_lJ_KffAARVDR6wZ1kZ8VvadaPqGBya_yw4Z4eQ130_provenance
a
np:Provenance
.
dgn-np:NP590198.RAsHvA_lJ_KffAARVDR6wZ1kZ8VvadaPqGBya_yw4Z4eQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP590198.RAsHvA_lJ_KffAARVDR6wZ1kZ8VvadaPqGBya_yw4Z4eQ130_assertion
{
miriam-gene:2048
a
ncit:C16612
.
lld:C0028326
a
ncit:C7057
.
dgn-gda:DGN3d573165c52c0df9cdf22200e28da5a0
sio:SIO_000628
miriam-gene:2048
,
lld:C0028326
;
a
sio:SIO_001121
.
}
dgn-np:NP590198.RAsHvA_lJ_KffAARVDR6wZ1kZ8VvadaPqGBya_yw4Z4eQ130_provenance
{
dgn-np:NP590198.RAsHvA_lJ_KffAARVDR6wZ1kZ8VvadaPqGBya_yw4Z4eQ130_assertion
dcterms:description
"[Cells transfected with constructs containing Noonan syndrome-associated RAF1 mutations showed increased in vitro kinase and ERK activation, and zebrafish embryos with morpholino knockdown of raf1 demonstrated the need for raf1 for the development of normal myocardial structure and 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:17603482
;
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:NP590198.RAsHvA_lJ_KffAARVDR6wZ1kZ8VvadaPqGBya_yw4Z4eQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:55+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" .
}