@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP272957.RALPWzDmwL-hQA6HIdiUjifw7hW_9vtgoT--gLXSl_-fk
> .
@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:NP272957.RALPWzDmwL-hQA6HIdiUjifw7hW_9vtgoT--gLXSl_-fk130_head
{
this:
np:hasAssertion
dgn-np:NP272957.RALPWzDmwL-hQA6HIdiUjifw7hW_9vtgoT--gLXSl_-fk130_assertion
;
np:hasProvenance
dgn-np:NP272957.RALPWzDmwL-hQA6HIdiUjifw7hW_9vtgoT--gLXSl_-fk130_provenance
;
np:hasPublicationInfo
dgn-np:NP272957.RALPWzDmwL-hQA6HIdiUjifw7hW_9vtgoT--gLXSl_-fk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP272957.RALPWzDmwL-hQA6HIdiUjifw7hW_9vtgoT--gLXSl_-fk130_assertion
a
np:Assertion
.
dgn-np:NP272957.RALPWzDmwL-hQA6HIdiUjifw7hW_9vtgoT--gLXSl_-fk130_provenance
a
np:Provenance
.
dgn-np:NP272957.RALPWzDmwL-hQA6HIdiUjifw7hW_9vtgoT--gLXSl_-fk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP272957.RALPWzDmwL-hQA6HIdiUjifw7hW_9vtgoT--gLXSl_-fk130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C1140680
a
ncit:C7057
.
dgn-gda:DGN9e199527fe66f8a42c104021fc498676
sio:SIO_000628
miriam-gene:672
,
lld:C1140680
;
a
sio:SIO_001121
.
}
dgn-np:NP272957.RALPWzDmwL-hQA6HIdiUjifw7hW_9vtgoT--gLXSl_-fk130_provenance
{
dgn-np:NP272957.RALPWzDmwL-hQA6HIdiUjifw7hW_9vtgoT--gLXSl_-fk130_assertion
dcterms:description
"[Our results suggest that BRCA1 and BRCA2 may be sufficient to explain the majority of familial ovarian cancer and that families without mutations can be explained by sensitivity of mutation testing and chance clusters of sporadic cases.]. 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:10642429
;
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:NP272957.RALPWzDmwL-hQA6HIdiUjifw7hW_9vtgoT--gLXSl_-fk130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:49+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" .
}