@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc
> .
@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:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_head
{
this:
np:hasAssertion
dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_assertion
;
np:hasProvenance
dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_provenance
;
np:hasPublicationInfo
dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_assertion
a
np:Assertion
.
dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_provenance
a
np:Provenance
.
dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_assertion
{
miriam-gene:23047
a
ncit:C16612
.
lld:C0678222
a
ncit:C7057
.
dgn-gda:DGN96299f760089d66e364f39cb8fce1d61
sio:SIO_000628
miriam-gene:23047
,
lld:C0678222
;
a
sio:SIO_001121
.
}
dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_provenance
{
dgn-np:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_assertion
dcterms:description
"[The clinical significance of these findings is indicated by the observation that the BRCA2/APRIN interaction is compromised by BRCA2 missense variants of previously unknown significance and that APRIN expression levels are associated with histological grade in breast cancer and the outcome of breast cancer patients treated with DNA-damaging chemotherapy.]. 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:22293751
;
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:NP668416.RABe2nfrryYb_S6OY2KPhsKsiUdZUKgtUKXEP0tdap4gc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:43+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" .
}