@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP280239.RA900QmUOU121OXdXRh2ObFisgw45lTdlOrxitHjS1txU
> .
@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:NP280239.RA900QmUOU121OXdXRh2ObFisgw45lTdlOrxitHjS1txU130_head
{
this:
np:hasAssertion
dgn-np:NP280239.RA900QmUOU121OXdXRh2ObFisgw45lTdlOrxitHjS1txU130_assertion
;
np:hasProvenance
dgn-np:NP280239.RA900QmUOU121OXdXRh2ObFisgw45lTdlOrxitHjS1txU130_provenance
;
np:hasPublicationInfo
dgn-np:NP280239.RA900QmUOU121OXdXRh2ObFisgw45lTdlOrxitHjS1txU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP280239.RA900QmUOU121OXdXRh2ObFisgw45lTdlOrxitHjS1txU130_assertion
a
np:Assertion
.
dgn-np:NP280239.RA900QmUOU121OXdXRh2ObFisgw45lTdlOrxitHjS1txU130_provenance
a
np:Provenance
.
dgn-np:NP280239.RA900QmUOU121OXdXRh2ObFisgw45lTdlOrxitHjS1txU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP280239.RA900QmUOU121OXdXRh2ObFisgw45lTdlOrxitHjS1txU130_assertion
{
miriam-gene:19
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN571343bf561ec29ca362f4e9ba1d407a
sio:SIO_000628
miriam-gene:19
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP280239.RA900QmUOU121OXdXRh2ObFisgw45lTdlOrxitHjS1txU130_provenance
{
dgn-np:NP280239.RA900QmUOU121OXdXRh2ObFisgw45lTdlOrxitHjS1txU130_assertion
dcterms:description
"[These studies showed that two SNPs in the COMT distal promoter were associated with breast cancer risk reduction in two of three case control studies, compatible with the results of functional genomic experiments, suggesting a role for MB-COMT in breast cancer risk.]. 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:18632656
;
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:NP280239.RA900QmUOU121OXdXRh2ObFisgw45lTdlOrxitHjS1txU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:38+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" .
}