@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk
> .
@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:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_head
{
this:
np:hasAssertion
dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_assertion
;
np:hasProvenance
dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_provenance
;
np:hasPublicationInfo
dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_assertion
a
np:Assertion
.
dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_provenance
a
np:Provenance
.
dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_assertion
{
miriam-gene:1588
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN9d02f37e7ec7fd273fa560822d1359c2
sio:SIO_000628
miriam-gene:1588
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_provenance
{
dgn-np:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_assertion
dct:description
"[Pairwise analysis showed that combinations of the ERalpha G allele with the homozygous Trp genotype of CYP19A1 codon 39 (rs2236722), the methionine (Met) allele of COMT codon 158 (rs4680) or Pro allele of p53 codon 72 (rs1042522) were more frequent in ER-positive than ER-negative breast cancer, especially in patients less than 50-year old.]. 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:18820009
;
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:NP46158.RAnuQpy7vBTE4eNI22yGccgwZGsH0DouTbvQHwO3FUdBk130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:21+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}