@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM
> .
@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:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_head
{
this:
np:hasAssertion
dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_assertion
;
np:hasProvenance
dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_provenance
;
np:hasPublicationInfo
dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_assertion
a
np:Assertion
.
dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_provenance
a
np:Provenance
.
dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C1333990
a
ncit:C7057
.
dgn-gda:DGN8fa68d261b15d4ecdfe53672745252a6
sio:SIO_000628
miriam-gene:672
,
lld:C1333990
;
a
sio:SIO_001121
.
}
dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_provenance
{
dgn-np:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_assertion
dcterms:description
"[At least one of ten patients with ovarian cancer is estimated to develop their tumor because of heredity with the breast and ovarian cancer syndrome due to mutations in the BRCA1 and BRCA2 genes and hereditary nonpolyposis colorectal cancer (HNPCC) being the major genetic causes.]. 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:17343610
;
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:NP597681.RAYcxIkXJrdiWP8Q4GY83K_Ezs7O91z0KNO7mqahJHttM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:16+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" .
}