@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg
> .
@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/v3.0.0/void/
> .
dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_head
{
this:
np:hasAssertion
dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_assertion
;
np:hasProvenance
dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_provenance
;
np:hasPublicationInfo
dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_assertion
a
np:Assertion
.
dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_provenance
a
np:Provenance
.
dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_assertion
{
miriam-gene:860
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN1d9ad98ebe31957da0359be97bf6bf04
sio:SIO_000628
miriam-gene:860
,
lld:C0006826
;
a
sio:SIO_001122
.
}
dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_provenance
{
dgn-np:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_assertion
dcterms:description
"[A Runx2 binding site was reported to be functional only in the minor, disease associated allele of rs2981578, resulting in increased expression of FGFR2 in cancers from patients homozygous for that allele.]. 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:24265722
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP284537.RAk4XzZtiZOqEuvuQRyxmKYY5RWl6wDhoP36KjgFQ-Ttg130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:40:22+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}