@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP77848.RADC0Wxlou4ad8TNun-X00b0vIjCoABxKzfiKVwcsyGoM
> .
@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:NP77848.RADC0Wxlou4ad8TNun-X00b0vIjCoABxKzfiKVwcsyGoM130_head
{
this:
np:hasAssertion
dgn-np:NP77848.RADC0Wxlou4ad8TNun-X00b0vIjCoABxKzfiKVwcsyGoM130_assertion
;
np:hasProvenance
dgn-np:NP77848.RADC0Wxlou4ad8TNun-X00b0vIjCoABxKzfiKVwcsyGoM130_provenance
;
np:hasPublicationInfo
dgn-np:NP77848.RADC0Wxlou4ad8TNun-X00b0vIjCoABxKzfiKVwcsyGoM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP77848.RADC0Wxlou4ad8TNun-X00b0vIjCoABxKzfiKVwcsyGoM130_assertion
a
np:Assertion
.
dgn-np:NP77848.RADC0Wxlou4ad8TNun-X00b0vIjCoABxKzfiKVwcsyGoM130_provenance
a
np:Provenance
.
dgn-np:NP77848.RADC0Wxlou4ad8TNun-X00b0vIjCoABxKzfiKVwcsyGoM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP77848.RADC0Wxlou4ad8TNun-X00b0vIjCoABxKzfiKVwcsyGoM130_assertion
{
miriam-gene:22843
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN59bc8d18820c240b083db61e0175839a
sio:SIO_000628
miriam-gene:22843
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP77848.RADC0Wxlou4ad8TNun-X00b0vIjCoABxKzfiKVwcsyGoM130_provenance
{
dgn-np:NP77848.RADC0Wxlou4ad8TNun-X00b0vIjCoABxKzfiKVwcsyGoM130_assertion
dcterms: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:NP77848.RADC0Wxlou4ad8TNun-X00b0vIjCoABxKzfiKVwcsyGoM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:38+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" .
}