@prefix dc: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP81039.RAeTaKvl9uIIUx01fCP4f3hdQ_u2lihHmIbHMLaLTaPEA
> .
@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 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:NP81039.RAeTaKvl9uIIUx01fCP4f3hdQ_u2lihHmIbHMLaLTaPEA130_head
{
this:
np:hasAssertion
dgn-np:NP81039.RAeTaKvl9uIIUx01fCP4f3hdQ_u2lihHmIbHMLaLTaPEA130_assertion
;
np:hasProvenance
dgn-np:NP81039.RAeTaKvl9uIIUx01fCP4f3hdQ_u2lihHmIbHMLaLTaPEA130_provenance
;
np:hasPublicationInfo
dgn-np:NP81039.RAeTaKvl9uIIUx01fCP4f3hdQ_u2lihHmIbHMLaLTaPEA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP81039.RAeTaKvl9uIIUx01fCP4f3hdQ_u2lihHmIbHMLaLTaPEA130_assertion
a
np:Assertion
.
dgn-np:NP81039.RAeTaKvl9uIIUx01fCP4f3hdQ_u2lihHmIbHMLaLTaPEA130_provenance
a
np:Provenance
.
dgn-np:NP81039.RAeTaKvl9uIIUx01fCP4f3hdQ_u2lihHmIbHMLaLTaPEA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP81039.RAeTaKvl9uIIUx01fCP4f3hdQ_u2lihHmIbHMLaLTaPEA130_assertion
{
miriam-gene:9496
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNe2173d19346b6ce519a30e5618317c7d
sio:SIO_000628
miriam-gene:9496
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP81039.RAeTaKvl9uIIUx01fCP4f3hdQ_u2lihHmIbHMLaLTaPEA130_provenance
{
dgn-np:NP81039.RAeTaKvl9uIIUx01fCP4f3hdQ_u2lihHmIbHMLaLTaPEA130_assertion
dc:description
"[These findings suggest that single polymorphisms and combinations of polymorphisms within candidate oncogenes from the 17q23 amplicon may influence risk of breast cancer overall and possibly specific molecular subtypes of breast tumors.]. 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:19454617
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP81039.RAeTaKvl9uIIUx01fCP4f3hdQ_u2lihHmIbHMLaLTaPEA130_publicationInfo
{
this:
dc:created
"2014-10-02T12:32:40+02:00"^^
xsd:dateTime
;
dc:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dc:rightsHolder
dgn-void:IBIGroup
;
dc: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" .
}