@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU
> .
@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:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_head
{
this:
np:hasAssertion
dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_assertion
;
np:hasProvenance
dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_provenance
;
np:hasPublicationInfo
dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_assertion
a
np:Assertion
.
dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_provenance
a
np:Provenance
.
dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C1140680
a
ncit:C7057
.
dgn-gda:DGNfd7de3f4aa3ca185fe1a07f5009cacfe
sio:SIO_000628
miriam-gene:672
,
lld:C1140680
;
a
sio:SIO_001121
.
}
dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_provenance
{
dgn-np:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_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-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:NP527349.RAskUQEkzgi3Aq5pOOL49FudQ3wjPr3E0WKeXMXhdFHdU130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:43+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: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" .
}