@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP15803.RAjbc8AvAIbrpApyAVvMD13ukesIhZN7mtK1XnOVQsrZQ
> .
@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:NP15803.RAjbc8AvAIbrpApyAVvMD13ukesIhZN7mtK1XnOVQsrZQ130_head
{
this:
np:hasAssertion
dgn-np:NP15803.RAjbc8AvAIbrpApyAVvMD13ukesIhZN7mtK1XnOVQsrZQ130_assertion
;
np:hasProvenance
dgn-np:NP15803.RAjbc8AvAIbrpApyAVvMD13ukesIhZN7mtK1XnOVQsrZQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP15803.RAjbc8AvAIbrpApyAVvMD13ukesIhZN7mtK1XnOVQsrZQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP15803.RAjbc8AvAIbrpApyAVvMD13ukesIhZN7mtK1XnOVQsrZQ130_assertion
a
np:Assertion
.
dgn-np:NP15803.RAjbc8AvAIbrpApyAVvMD13ukesIhZN7mtK1XnOVQsrZQ130_provenance
a
np:Provenance
.
dgn-np:NP15803.RAjbc8AvAIbrpApyAVvMD13ukesIhZN7mtK1XnOVQsrZQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP15803.RAjbc8AvAIbrpApyAVvMD13ukesIhZN7mtK1XnOVQsrZQ130_assertion
{
miriam-gene:2263
a
ncit:C16612
.
lld:C1458155
a
ncit:C7057
.
dgn-gda:DGNaa77127fd3a0e23bacb812b648291a99
sio:SIO_000628
miriam-gene:2263
,
lld:C1458155
;
a
sio:SIO_001121
.
}
dgn-np:NP15803.RAjbc8AvAIbrpApyAVvMD13ukesIhZN7mtK1XnOVQsrZQ130_provenance
{
dgn-np:NP15803.RAjbc8AvAIbrpApyAVvMD13ukesIhZN7mtK1XnOVQsrZQ130_assertion
dcterms:description
"[We identified four SNPs in intron 2 of FGFR2 (which encodes a receptor tyrosine kinase and is amplified or overexpressed in some breast cancers) that were highly associated with breast cancer and confirmed this association in 1,776 affected individuals and 2,072 controls from three additional studies.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:17529973
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP15803.RAjbc8AvAIbrpApyAVvMD13ukesIhZN7mtK1XnOVQsrZQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:05+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" .
}