@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP405584.RA8Pu6Al2N_dIl997FdWZU2ot2AMtCpYNeoMonRwvfMio
> .
@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:NP405584.RA8Pu6Al2N_dIl997FdWZU2ot2AMtCpYNeoMonRwvfMio130_head
{
this:
np:hasAssertion
dgn-np:NP405584.RA8Pu6Al2N_dIl997FdWZU2ot2AMtCpYNeoMonRwvfMio130_assertion
;
np:hasProvenance
dgn-np:NP405584.RA8Pu6Al2N_dIl997FdWZU2ot2AMtCpYNeoMonRwvfMio130_provenance
;
np:hasPublicationInfo
dgn-np:NP405584.RA8Pu6Al2N_dIl997FdWZU2ot2AMtCpYNeoMonRwvfMio130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP405584.RA8Pu6Al2N_dIl997FdWZU2ot2AMtCpYNeoMonRwvfMio130_assertion
a
np:Assertion
.
dgn-np:NP405584.RA8Pu6Al2N_dIl997FdWZU2ot2AMtCpYNeoMonRwvfMio130_provenance
a
np:Provenance
.
dgn-np:NP405584.RA8Pu6Al2N_dIl997FdWZU2ot2AMtCpYNeoMonRwvfMio130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP405584.RA8Pu6Al2N_dIl997FdWZU2ot2AMtCpYNeoMonRwvfMio130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C1140680
a
ncit:C7057
.
dgn-gda:DGNacc503b460486ab5bc1a68fd4a9248ae
sio:SIO_000628
miriam-gene:672
,
lld:C1140680
;
a
sio:SIO_001121
.
}
dgn-np:NP405584.RA8Pu6Al2N_dIl997FdWZU2ot2AMtCpYNeoMonRwvfMio130_provenance
{
dgn-np:NP405584.RA8Pu6Al2N_dIl997FdWZU2ot2AMtCpYNeoMonRwvfMio130_assertion
dcterms:description
"[The high frequency of BRCA1 mutations in Polish women with ovarian cancer supports the recommendation that all Polish women with ovarian cancer should be offered testing for genetic susceptibility, and that counseling services be made available to them and to their relatives.]. 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:12918074
;
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:NP405584.RA8Pu6Al2N_dIl997FdWZU2ot2AMtCpYNeoMonRwvfMio130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:49+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" .
}