@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP292158.RAZJ3SATOFsjPBo9iyHI_XS53WhCvxEwvTD3lYOIW2qs8
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP292158.RAZJ3SATOFsjPBo9iyHI_XS53WhCvxEwvTD3lYOIW2qs8130_assertion
;
np:hasProvenance
dgn-np:NP292158.RAZJ3SATOFsjPBo9iyHI_XS53WhCvxEwvTD3lYOIW2qs8130_provenance
;
np:hasPublicationInfo
dgn-np:NP292158.RAZJ3SATOFsjPBo9iyHI_XS53WhCvxEwvTD3lYOIW2qs8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP292158.RAZJ3SATOFsjPBo9iyHI_XS53WhCvxEwvTD3lYOIW2qs8130_assertion
a
np:Assertion
.
dgn-np:NP292158.RAZJ3SATOFsjPBo9iyHI_XS53WhCvxEwvTD3lYOIW2qs8130_provenance
a
np:Provenance
.
dgn-np:NP292158.RAZJ3SATOFsjPBo9iyHI_XS53WhCvxEwvTD3lYOIW2qs8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP292158.RAZJ3SATOFsjPBo9iyHI_XS53WhCvxEwvTD3lYOIW2qs8130_assertion
{
miriam-gene:2263
a
ncit:C16612
.
lld:C0001193
a
ncit:C7057
.
dgn-gda:DGN9e4ecb3a7e54bb12b3e54d992bc8ec71
sio:SIO_000628
miriam-gene:2263
,
lld:C0001193
;
a
sio:SIO_001121
.
}
dgn-np:NP292158.RAZJ3SATOFsjPBo9iyHI_XS53WhCvxEwvTD3lYOIW2qs8130_provenance
{
dgn-np:NP292158.RAZJ3SATOFsjPBo9iyHI_XS53WhCvxEwvTD3lYOIW2qs8130_assertion
dcterms:description
"[Since our gene expression results suggested that novel signaling elicited by mutant FGFR2 might be associated with central nervous system (CNS) development and maintenance, we next investigated if DEGs found in AS cells were also altered in the CNS of an AS mouse model.]. 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:23593218
;
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:NP292158.RAZJ3SATOFsjPBo9iyHI_XS53WhCvxEwvTD3lYOIW2qs8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:46+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
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dgn-void:disgenetrdf
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}