@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM
> .
@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:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_head
{
this:
np:hasAssertion
dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_assertion
;
np:hasProvenance
dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_provenance
;
np:hasPublicationInfo
dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_assertion
a
np:Assertion
.
dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_provenance
a
np:Provenance
.
dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_assertion
{
miriam-gene:6899
a
ncit:C16612
.
lld:C0008487
a
ncit:C7057
.
dgn-gda:DGN4f68da490bd55f3cff4ea200ef63e00e
sio:SIO_000628
miriam-gene:6899
,
lld:C0008487
;
a
sio:SIO_001121
.
}
dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_provenance
{
dgn-np:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_assertion
dcterms:description
"[The aim of this study was to attempt to identify the molecular genetic events that are responsible for the pathogenesis of chordomas with particular focus on the FGFR signalling pathway on the basis of the evidence in the ascidian and Xenopus models that the expression of brachyury requires the activation of this pathway.]. 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:19407855
;
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:NP306135.RAPGv7pl75JOnmwSRJYh6qP-rMxzKDVo45Tc0RI2UPyRM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:55+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
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"v2.1.0" .
}