@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP339068.RAD9kfMRH0AGOA51G7OTOUHUSkHRsKMCL247Abf-TVVCI
> .
@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:NP339068.RAD9kfMRH0AGOA51G7OTOUHUSkHRsKMCL247Abf-TVVCI130_head
{
this:
np:hasAssertion
dgn-np:NP339068.RAD9kfMRH0AGOA51G7OTOUHUSkHRsKMCL247Abf-TVVCI130_assertion
;
np:hasProvenance
dgn-np:NP339068.RAD9kfMRH0AGOA51G7OTOUHUSkHRsKMCL247Abf-TVVCI130_provenance
;
np:hasPublicationInfo
dgn-np:NP339068.RAD9kfMRH0AGOA51G7OTOUHUSkHRsKMCL247Abf-TVVCI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP339068.RAD9kfMRH0AGOA51G7OTOUHUSkHRsKMCL247Abf-TVVCI130_assertion
a
np:Assertion
.
dgn-np:NP339068.RAD9kfMRH0AGOA51G7OTOUHUSkHRsKMCL247Abf-TVVCI130_provenance
a
np:Provenance
.
dgn-np:NP339068.RAD9kfMRH0AGOA51G7OTOUHUSkHRsKMCL247Abf-TVVCI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP339068.RAD9kfMRH0AGOA51G7OTOUHUSkHRsKMCL247Abf-TVVCI130_assertion
{
miriam-gene:1577
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN67cc3112ce232b4c975350eb13cdeac8
sio:SIO_000628
miriam-gene:1577
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP339068.RAD9kfMRH0AGOA51G7OTOUHUSkHRsKMCL247Abf-TVVCI130_provenance
{
dgn-np:NP339068.RAD9kfMRH0AGOA51G7OTOUHUSkHRsKMCL247Abf-TVVCI130_assertion
dcterms:description
"[Genotypic variants of CYP1A1 have been associated with increased aryl hydrocarbon hydroxylase activity, and some epidemiological studies suggest that women with the variant genotype(s) are at increased risk for breast cancer.]. 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:9485019
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP339068.RAD9kfMRH0AGOA51G7OTOUHUSkHRsKMCL247Abf-TVVCI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:19+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" .
}