@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP503271.RAomDJ6MXW3eF2EM-mbGW-NVhg3_AmMm8RXxHDU5zoJfo
> .
@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:NP503271.RAomDJ6MXW3eF2EM-mbGW-NVhg3_AmMm8RXxHDU5zoJfo130_head
{
this:
np:hasAssertion
dgn-np:NP503271.RAomDJ6MXW3eF2EM-mbGW-NVhg3_AmMm8RXxHDU5zoJfo130_assertion
;
np:hasProvenance
dgn-np:NP503271.RAomDJ6MXW3eF2EM-mbGW-NVhg3_AmMm8RXxHDU5zoJfo130_provenance
;
np:hasPublicationInfo
dgn-np:NP503271.RAomDJ6MXW3eF2EM-mbGW-NVhg3_AmMm8RXxHDU5zoJfo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP503271.RAomDJ6MXW3eF2EM-mbGW-NVhg3_AmMm8RXxHDU5zoJfo130_assertion
a
np:Assertion
.
dgn-np:NP503271.RAomDJ6MXW3eF2EM-mbGW-NVhg3_AmMm8RXxHDU5zoJfo130_provenance
a
np:Provenance
.
dgn-np:NP503271.RAomDJ6MXW3eF2EM-mbGW-NVhg3_AmMm8RXxHDU5zoJfo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP503271.RAomDJ6MXW3eF2EM-mbGW-NVhg3_AmMm8RXxHDU5zoJfo130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGNbac5fc975b7a1f18526f9b7e875ec1f9
sio:SIO_000628
miriam-gene:672
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP503271.RAomDJ6MXW3eF2EM-mbGW-NVhg3_AmMm8RXxHDU5zoJfo130_provenance
{
dgn-np:NP503271.RAomDJ6MXW3eF2EM-mbGW-NVhg3_AmMm8RXxHDU5zoJfo130_assertion
dcterms:description
"[The hereditary breast and ovarian cancer syndrome, primarily due to mutations in BRCA1 and BRCA2, is the main cause of heredity, but also the hereditary nonpolyposis colorectal cancer (HNPCC) syndrome confers an increased risk of ovarian cancer.]. 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:16360201
;
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:NP503271.RAomDJ6MXW3eF2EM-mbGW-NVhg3_AmMm8RXxHDU5zoJfo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:00+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" .
}