@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP858490.RA-zYcQeGNtnln2kyC4XklOaPEN9ch-WdGgBszJJe3cF4
> .
@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:NP858490.RA-zYcQeGNtnln2kyC4XklOaPEN9ch-WdGgBszJJe3cF4130_head
{
this:
np:hasAssertion
dgn-np:NP858490.RA-zYcQeGNtnln2kyC4XklOaPEN9ch-WdGgBszJJe3cF4130_assertion
;
np:hasProvenance
dgn-np:NP858490.RA-zYcQeGNtnln2kyC4XklOaPEN9ch-WdGgBszJJe3cF4130_provenance
;
np:hasPublicationInfo
dgn-np:NP858490.RA-zYcQeGNtnln2kyC4XklOaPEN9ch-WdGgBszJJe3cF4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP858490.RA-zYcQeGNtnln2kyC4XklOaPEN9ch-WdGgBszJJe3cF4130_assertion
a
np:Assertion
.
dgn-np:NP858490.RA-zYcQeGNtnln2kyC4XklOaPEN9ch-WdGgBszJJe3cF4130_provenance
a
np:Provenance
.
dgn-np:NP858490.RA-zYcQeGNtnln2kyC4XklOaPEN9ch-WdGgBszJJe3cF4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP858490.RA-zYcQeGNtnln2kyC4XklOaPEN9ch-WdGgBszJJe3cF4130_assertion
{
miriam-gene:672
a
ncit:C16612
.
lld:C0206697
a
ncit:C7057
.
dgn-gda:DGNc9336c0445a71783e9d89a90044edfa9
sio:SIO_000628
miriam-gene:672
,
lld:C0206697
;
a
sio:SIO_001121
.
}
dgn-np:NP858490.RA-zYcQeGNtnln2kyC4XklOaPEN9ch-WdGgBszJJe3cF4130_provenance
{
dgn-np:NP858490.RA-zYcQeGNtnln2kyC4XklOaPEN9ch-WdGgBszJJe3cF4130_assertion
dcterms:description
"[Ovarian surfaces were scraped to retrieve OSE cells from 56 women at hereditary high risk for female adnexal carcinoma, of whom 33 are BRCA1 and four are BRCA2 mutation carriers (Predisposed OSE, POSE) and from 26 women without such risk (Non Predisposed OSE, NPOSE).]. 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:14984947
;
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:NP858490.RA-zYcQeGNtnln2kyC4XklOaPEN9ch-WdGgBszJJe3cF4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:45+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" .
}