@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP767185.RAgyVGF9xek3a-2ZiD4fGPGM99081JrwdMrYNG0VWr0Xw
> .
@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:NP767185.RAgyVGF9xek3a-2ZiD4fGPGM99081JrwdMrYNG0VWr0Xw130_head
{
this:
np:hasAssertion
dgn-np:NP767185.RAgyVGF9xek3a-2ZiD4fGPGM99081JrwdMrYNG0VWr0Xw130_assertion
;
np:hasProvenance
dgn-np:NP767185.RAgyVGF9xek3a-2ZiD4fGPGM99081JrwdMrYNG0VWr0Xw130_provenance
;
np:hasPublicationInfo
dgn-np:NP767185.RAgyVGF9xek3a-2ZiD4fGPGM99081JrwdMrYNG0VWr0Xw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP767185.RAgyVGF9xek3a-2ZiD4fGPGM99081JrwdMrYNG0VWr0Xw130_assertion
a
np:Assertion
.
dgn-np:NP767185.RAgyVGF9xek3a-2ZiD4fGPGM99081JrwdMrYNG0VWr0Xw130_provenance
a
np:Provenance
.
dgn-np:NP767185.RAgyVGF9xek3a-2ZiD4fGPGM99081JrwdMrYNG0VWr0Xw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP767185.RAgyVGF9xek3a-2ZiD4fGPGM99081JrwdMrYNG0VWr0Xw130_assertion
{
miriam-gene:9360
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN3259ae143726cb71cfd6303bd9f39b23
sio:SIO_000628
miriam-gene:9360
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP767185.RAgyVGF9xek3a-2ZiD4fGPGM99081JrwdMrYNG0VWr0Xw130_provenance
{
dgn-np:NP767185.RAgyVGF9xek3a-2ZiD4fGPGM99081JrwdMrYNG0VWr0Xw130_assertion
dcterms:description
"[Previous studies have suggested that minor alleles for ERCC4 rs744154, TNF rs361525, CASP10 rs13010627, PGR rs1042838, and BID rs8190315 may influence breast cancer risk, but the evidence is inconclusive due to their small sample size.]. 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:19423537
;
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:NP767185.RAgyVGF9xek3a-2ZiD4fGPGM99081JrwdMrYNG0VWr0Xw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:44+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" .
}