@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP53213.RAABtBZxznNGZxmhxDx1cQvGlIpyYF_BYVa-_qbgPIhDA
> .
@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:NP53213.RAABtBZxznNGZxmhxDx1cQvGlIpyYF_BYVa-_qbgPIhDA130_head
{
this:
np:hasAssertion
dgn-np:NP53213.RAABtBZxznNGZxmhxDx1cQvGlIpyYF_BYVa-_qbgPIhDA130_assertion
;
np:hasProvenance
dgn-np:NP53213.RAABtBZxznNGZxmhxDx1cQvGlIpyYF_BYVa-_qbgPIhDA130_provenance
;
np:hasPublicationInfo
dgn-np:NP53213.RAABtBZxznNGZxmhxDx1cQvGlIpyYF_BYVa-_qbgPIhDA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP53213.RAABtBZxznNGZxmhxDx1cQvGlIpyYF_BYVa-_qbgPIhDA130_assertion
a
np:Assertion
.
dgn-np:NP53213.RAABtBZxznNGZxmhxDx1cQvGlIpyYF_BYVa-_qbgPIhDA130_provenance
a
np:Provenance
.
dgn-np:NP53213.RAABtBZxznNGZxmhxDx1cQvGlIpyYF_BYVa-_qbgPIhDA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP53213.RAABtBZxznNGZxmhxDx1cQvGlIpyYF_BYVa-_qbgPIhDA130_assertion
{
miriam-gene:5241
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN64c1907a590a6dc9b61aeb3a46ad1628
sio:SIO_000628
miriam-gene:5241
,
lld:C0006142
;
a
sio:SIO_001122
.
}
dgn-np:NP53213.RAABtBZxznNGZxmhxDx1cQvGlIpyYF_BYVa-_qbgPIhDA130_provenance
{
dgn-np:NP53213.RAABtBZxznNGZxmhxDx1cQvGlIpyYF_BYVa-_qbgPIhDA130_assertion
dcterms:description
"[our data provide persuasive evidence against an overall association between invasive breast cancer risk and ERCC4 rs744154, TNF rs361525, CASP10 rs13010627, PGR rs1042838, and BID rs8190315 genotypes among women of European 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:19423537
;
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:NP53213.RAABtBZxznNGZxmhxDx1cQvGlIpyYF_BYVa-_qbgPIhDA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:24+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" .
}