@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP539427.RAupc29ozN6uDksTpLxwuJH_ci5RSyJ10FjA4sh83hQHg
> .
@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:NP539427.RAupc29ozN6uDksTpLxwuJH_ci5RSyJ10FjA4sh83hQHg130_head
{
this:
np:hasAssertion
dgn-np:NP539427.RAupc29ozN6uDksTpLxwuJH_ci5RSyJ10FjA4sh83hQHg130_assertion
;
np:hasProvenance
dgn-np:NP539427.RAupc29ozN6uDksTpLxwuJH_ci5RSyJ10FjA4sh83hQHg130_provenance
;
np:hasPublicationInfo
dgn-np:NP539427.RAupc29ozN6uDksTpLxwuJH_ci5RSyJ10FjA4sh83hQHg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP539427.RAupc29ozN6uDksTpLxwuJH_ci5RSyJ10FjA4sh83hQHg130_assertion
a
np:Assertion
.
dgn-np:NP539427.RAupc29ozN6uDksTpLxwuJH_ci5RSyJ10FjA4sh83hQHg130_provenance
a
np:Provenance
.
dgn-np:NP539427.RAupc29ozN6uDksTpLxwuJH_ci5RSyJ10FjA4sh83hQHg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP539427.RAupc29ozN6uDksTpLxwuJH_ci5RSyJ10FjA4sh83hQHg130_assertion
{
miriam-gene:84464
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNe9a4cad16d271efd3740ffecc91c6957
sio:SIO_000628
miriam-gene:84464
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP539427.RAupc29ozN6uDksTpLxwuJH_ci5RSyJ10FjA4sh83hQHg130_provenance
{
dgn-np:NP539427.RAupc29ozN6uDksTpLxwuJH_ci5RSyJ10FjA4sh83hQHg130_assertion
dcterms:description
"[Overall, while the results of this study do not identify clearly pathogenic mutations of SLX4 contributing to breast cancer risk, further genetic analysis, combined with functional assays of the identified rare variants, may be warranted to conclusively assess the potential link with the disease.]. 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:22401137
;
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:NP539427.RAupc29ozN6uDksTpLxwuJH_ci5RSyJ10FjA4sh83hQHg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:25+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" .
}