@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP279994.RAFGQhNo2DYL0LEy5Y9FOrDRGJnDJNTGEu-25-uW2lIM4
> .
@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:NP279994.RAFGQhNo2DYL0LEy5Y9FOrDRGJnDJNTGEu-25-uW2lIM4130_head
{
this:
np:hasAssertion
dgn-np:NP279994.RAFGQhNo2DYL0LEy5Y9FOrDRGJnDJNTGEu-25-uW2lIM4130_assertion
;
np:hasProvenance
dgn-np:NP279994.RAFGQhNo2DYL0LEy5Y9FOrDRGJnDJNTGEu-25-uW2lIM4130_provenance
;
np:hasPublicationInfo
dgn-np:NP279994.RAFGQhNo2DYL0LEy5Y9FOrDRGJnDJNTGEu-25-uW2lIM4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP279994.RAFGQhNo2DYL0LEy5Y9FOrDRGJnDJNTGEu-25-uW2lIM4130_assertion
a
np:Assertion
.
dgn-np:NP279994.RAFGQhNo2DYL0LEy5Y9FOrDRGJnDJNTGEu-25-uW2lIM4130_provenance
a
np:Provenance
.
dgn-np:NP279994.RAFGQhNo2DYL0LEy5Y9FOrDRGJnDJNTGEu-25-uW2lIM4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP279994.RAFGQhNo2DYL0LEy5Y9FOrDRGJnDJNTGEu-25-uW2lIM4130_assertion
{
miriam-gene:580
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGNc0e9e739b3085e2d1f4764d9d89ba523
sio:SIO_000628
miriam-gene:580
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP279994.RAFGQhNo2DYL0LEy5Y9FOrDRGJnDJNTGEu-25-uW2lIM4130_provenance
{
dgn-np:NP279994.RAFGQhNo2DYL0LEy5Y9FOrDRGJnDJNTGEu-25-uW2lIM4130_assertion
dcterms:description
"[Expression of NH(2) terminally truncated BARD1 was correlated with advanced stage of cancer, and expression of spliced isoforms was typical for clear cell carcinoma, the ovarian cancer with worst prognosis, suggesting a role of BARD1 isoforms in cancer progression.]. 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:18089818
;
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:NP279994.RAFGQhNo2DYL0LEy5Y9FOrDRGJnDJNTGEu-25-uW2lIM4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:38+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" .
}