@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP45886.RA7gXkDralTPktmi6hdkZJZif39WjoVYtgNemtHeSPdoY
> .
@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:NP45886.RA7gXkDralTPktmi6hdkZJZif39WjoVYtgNemtHeSPdoY130_head
{
this:
np:hasAssertion
dgn-np:NP45886.RA7gXkDralTPktmi6hdkZJZif39WjoVYtgNemtHeSPdoY130_assertion
;
np:hasProvenance
dgn-np:NP45886.RA7gXkDralTPktmi6hdkZJZif39WjoVYtgNemtHeSPdoY130_provenance
;
np:hasPublicationInfo
dgn-np:NP45886.RA7gXkDralTPktmi6hdkZJZif39WjoVYtgNemtHeSPdoY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP45886.RA7gXkDralTPktmi6hdkZJZif39WjoVYtgNemtHeSPdoY130_assertion
a
np:Assertion
.
dgn-np:NP45886.RA7gXkDralTPktmi6hdkZJZif39WjoVYtgNemtHeSPdoY130_provenance
a
np:Provenance
.
dgn-np:NP45886.RA7gXkDralTPktmi6hdkZJZif39WjoVYtgNemtHeSPdoY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP45886.RA7gXkDralTPktmi6hdkZJZif39WjoVYtgNemtHeSPdoY130_assertion
{
miriam-gene:1545
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN6f7702e646d89bdc1e6f6d0f433eb640
sio:SIO_000628
miriam-gene:1545
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP45886.RA7gXkDralTPktmi6hdkZJZif39WjoVYtgNemtHeSPdoY130_provenance
{
dgn-np:NP45886.RA7gXkDralTPktmi6hdkZJZif39WjoVYtgNemtHeSPdoY130_assertion
dcterms:description
"[Our results suggest that the codon 432 polymorphism of the CYP1B1 gene is associated with increased risk of breast cancer and is particularly involved in breast cancer risk in premenopausal women of African descent.]. 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:19208203
;
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:NP45886.RA7gXkDralTPktmi6hdkZJZif39WjoVYtgNemtHeSPdoY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:21+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" .
}