@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP910605.RA5SGPoC3AqxzjEG_1KV7e9MlOpEn30YRkoNAzraPQPPc
> .
@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:NP910605.RA5SGPoC3AqxzjEG_1KV7e9MlOpEn30YRkoNAzraPQPPc130_head
{
this:
np:hasAssertion
dgn-np:NP910605.RA5SGPoC3AqxzjEG_1KV7e9MlOpEn30YRkoNAzraPQPPc130_assertion
;
np:hasProvenance
dgn-np:NP910605.RA5SGPoC3AqxzjEG_1KV7e9MlOpEn30YRkoNAzraPQPPc130_provenance
;
np:hasPublicationInfo
dgn-np:NP910605.RA5SGPoC3AqxzjEG_1KV7e9MlOpEn30YRkoNAzraPQPPc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP910605.RA5SGPoC3AqxzjEG_1KV7e9MlOpEn30YRkoNAzraPQPPc130_assertion
a
np:Assertion
.
dgn-np:NP910605.RA5SGPoC3AqxzjEG_1KV7e9MlOpEn30YRkoNAzraPQPPc130_provenance
a
np:Provenance
.
dgn-np:NP910605.RA5SGPoC3AqxzjEG_1KV7e9MlOpEn30YRkoNAzraPQPPc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP910605.RA5SGPoC3AqxzjEG_1KV7e9MlOpEn30YRkoNAzraPQPPc130_assertion
{
miriam-gene:675
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN9f2fa500fe87e848ae84c68463fd55c6
sio:SIO_000628
miriam-gene:675
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP910605.RA5SGPoC3AqxzjEG_1KV7e9MlOpEn30YRkoNAzraPQPPc130_provenance
{
dgn-np:NP910605.RA5SGPoC3AqxzjEG_1KV7e9MlOpEn30YRkoNAzraPQPPc130_assertion
dcterms:description
"[This suggests that in contrast to hereditary disease, BRCA1 and BRCA2 are not commonly involved in sporadic ovarian cancer and may indicate that there are two distinct pathways for the development 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:11598149
;
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:NP910605.RA5SGPoC3AqxzjEG_1KV7e9MlOpEn30YRkoNAzraPQPPc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:19+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" .
}