@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP359484.RANPfFf9hSZhAXnC_azaIUfwqZuN9vVnJjDyyRuDo_3FY
> .
@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/
> .
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{
this:
np:hasAssertion
dgn-np:NP359484.RANPfFf9hSZhAXnC_azaIUfwqZuN9vVnJjDyyRuDo_3FY130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP359484.RANPfFf9hSZhAXnC_azaIUfwqZuN9vVnJjDyyRuDo_3FY130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
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a
np:Provenance
.
dgn-np:NP359484.RANPfFf9hSZhAXnC_azaIUfwqZuN9vVnJjDyyRuDo_3FY130_publicationInfo
a
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{
miriam-gene:672
a
ncit:C16612
.
lld:C0029925
a
ncit:C7057
.
dgn-gda:DGNd2d3b8865b02d4af6b772cd8d56e33d8
sio:SIO_000628
miriam-gene:672
,
lld:C0029925
;
a
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.
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dgn-np:NP359484.RANPfFf9hSZhAXnC_azaIUfwqZuN9vVnJjDyyRuDo_3FY130_provenance
{
dgn-np:NP359484.RANPfFf9hSZhAXnC_azaIUfwqZuN9vVnJjDyyRuDo_3FY130_assertion
dcterms:description
"[We used complementary DNA (cDNA) microarrays to compare gene expression patterns in ovarian cancers associated with BRCA1 or BRCA2 mutations with gene expression patterns in sporadic epithelial ovarian cancers and to identify patterns common to both hereditary and sporadic tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_literature
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sio:SIO_000772
miriam-pubmed:12096084
;
prov:wasDerivedFrom
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;
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 .
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dgn-np:NP359484.RANPfFf9hSZhAXnC_azaIUfwqZuN9vVnJjDyyRuDo_3FY130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
;
prv:usedData
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
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> , <
http://orcid.org/0000-0003-1244-7654
> ;
pav:createdBy
<
http://orcid.org/0000-0003-0169-8159
> ;
pav:version
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"v4.0.0" .
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