@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP571111.RAvK3rfXrTNs9Vd41BwwbdMHSoysFdG7tUiSm0rYR-lQE
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP571111.RAvK3rfXrTNs9Vd41BwwbdMHSoysFdG7tUiSm0rYR-lQE130_head
{
this:
np:hasAssertion
dgn-np:NP571111.RAvK3rfXrTNs9Vd41BwwbdMHSoysFdG7tUiSm0rYR-lQE130_assertion
;
np:hasProvenance
dgn-np:NP571111.RAvK3rfXrTNs9Vd41BwwbdMHSoysFdG7tUiSm0rYR-lQE130_provenance
;
np:hasPublicationInfo
dgn-np:NP571111.RAvK3rfXrTNs9Vd41BwwbdMHSoysFdG7tUiSm0rYR-lQE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP571111.RAvK3rfXrTNs9Vd41BwwbdMHSoysFdG7tUiSm0rYR-lQE130_assertion
a
np:Assertion
.
dgn-np:NP571111.RAvK3rfXrTNs9Vd41BwwbdMHSoysFdG7tUiSm0rYR-lQE130_provenance
a
np:Provenance
.
dgn-np:NP571111.RAvK3rfXrTNs9Vd41BwwbdMHSoysFdG7tUiSm0rYR-lQE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP571111.RAvK3rfXrTNs9Vd41BwwbdMHSoysFdG7tUiSm0rYR-lQE130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0677886
a
ncit:C7057
.
dgn-gda:DGN02a36b5b8e3bee6284d9483d42e90499
sio:SIO_000628
miriam-gene:675
,
lld:C0677886
;
a
sio:SIO_001121
.
}
dgn-np:NP571111.RAvK3rfXrTNs9Vd41BwwbdMHSoysFdG7tUiSm0rYR-lQE130_provenance
{
dgn-np:NP571111.RAvK3rfXrTNs9Vd41BwwbdMHSoysFdG7tUiSm0rYR-lQE130_assertion
dcterms:description
"[The identification of germ-line mutations in 2 genes (BRCA1 and BRCA2) responsible for the majority of hereditary ovarian cancers has led an increasing number of women carriers of these mutations to undergo prophylactic oophorectomy (PO) to reduce their risk of subsequent ovarian carcinoma.]. 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:17001151
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP571111.RAvK3rfXrTNs9Vd41BwwbdMHSoysFdG7tUiSm0rYR-lQE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:03+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}