@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP564032.RAyqcsILvKQsR627lfBsX6SGu-3U-62N7NBelDaECTegQ
> .
@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:NP564032.RAyqcsILvKQsR627lfBsX6SGu-3U-62N7NBelDaECTegQ130_head
{
this:
np:hasAssertion
dgn-np:NP564032.RAyqcsILvKQsR627lfBsX6SGu-3U-62N7NBelDaECTegQ130_assertion
;
np:hasProvenance
dgn-np:NP564032.RAyqcsILvKQsR627lfBsX6SGu-3U-62N7NBelDaECTegQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP564032.RAyqcsILvKQsR627lfBsX6SGu-3U-62N7NBelDaECTegQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP564032.RAyqcsILvKQsR627lfBsX6SGu-3U-62N7NBelDaECTegQ130_assertion
a
np:Assertion
.
dgn-np:NP564032.RAyqcsILvKQsR627lfBsX6SGu-3U-62N7NBelDaECTegQ130_provenance
a
np:Provenance
.
dgn-np:NP564032.RAyqcsILvKQsR627lfBsX6SGu-3U-62N7NBelDaECTegQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP564032.RAyqcsILvKQsR627lfBsX6SGu-3U-62N7NBelDaECTegQ130_assertion
{
miriam-gene:116840
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGN8fe3ab911357952e4d1c655209951d70
sio:SIO_000628
miriam-gene:116840
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP564032.RAyqcsILvKQsR627lfBsX6SGu-3U-62N7NBelDaECTegQ130_provenance
{
dgn-np:NP564032.RAyqcsILvKQsR627lfBsX6SGu-3U-62N7NBelDaECTegQ130_assertion
dcterms:description
"[Furthermore, women harboring both at-risk haplotype GTAT of Nek2 and protective haplotype CATCG of centrobin were linked with decreased breast cancer risk, suggesting that the association between genetic variants of Nek2 and increased breast cancer risk was modified by genetic variants of centrobin.]. 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:23001753
;
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:NP564032.RAyqcsILvKQsR627lfBsX6SGu-3U-62N7NBelDaECTegQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}