@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP610282.RAGuSiW_2mvbVvZFJQBM9c5llGJMGhCLB-A6XpLY5nUUU
> .
@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:NP610282.RAGuSiW_2mvbVvZFJQBM9c5llGJMGhCLB-A6XpLY5nUUU130_head
{
this:
np:hasAssertion
dgn-np:NP610282.RAGuSiW_2mvbVvZFJQBM9c5llGJMGhCLB-A6XpLY5nUUU130_assertion
;
np:hasProvenance
dgn-np:NP610282.RAGuSiW_2mvbVvZFJQBM9c5llGJMGhCLB-A6XpLY5nUUU130_provenance
;
np:hasPublicationInfo
dgn-np:NP610282.RAGuSiW_2mvbVvZFJQBM9c5llGJMGhCLB-A6XpLY5nUUU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP610282.RAGuSiW_2mvbVvZFJQBM9c5llGJMGhCLB-A6XpLY5nUUU130_assertion
a
np:Assertion
.
dgn-np:NP610282.RAGuSiW_2mvbVvZFJQBM9c5llGJMGhCLB-A6XpLY5nUUU130_provenance
a
np:Provenance
.
dgn-np:NP610282.RAGuSiW_2mvbVvZFJQBM9c5llGJMGhCLB-A6XpLY5nUUU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP610282.RAGuSiW_2mvbVvZFJQBM9c5llGJMGhCLB-A6XpLY5nUUU130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C1333600
a
ncit:C7057
.
dgn-gda:DGN91639f446feedb98bb571277b28df17d
sio:SIO_000628
miriam-gene:7248
,
lld:C1333600
;
a
sio:SIO_001121
.
}
dgn-np:NP610282.RAGuSiW_2mvbVvZFJQBM9c5llGJMGhCLB-A6XpLY5nUUU130_provenance
{
dgn-np:NP610282.RAGuSiW_2mvbVvZFJQBM9c5llGJMGhCLB-A6XpLY5nUUU130_assertion
dcterms:description
"[Several loci on chromosome 13q show high frequencies of LOH in BRCA1 related ovarian and fallopian tube cancer, and may therefore harbour putative tumour suppressor genes involved in the carcinogenesis of this particular type of hereditary 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:12354934
;
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:NP610282.RAGuSiW_2mvbVvZFJQBM9c5llGJMGhCLB-A6XpLY5nUUU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:06+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" .
}