@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP938546.RA1Xkh9NTyd2xxSDJy5tZwYYh29drvxTe5MKTL6Z6b2gU
> .
@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:NP938546.RA1Xkh9NTyd2xxSDJy5tZwYYh29drvxTe5MKTL6Z6b2gU130_head
{
this:
np:hasAssertion
dgn-np:NP938546.RA1Xkh9NTyd2xxSDJy5tZwYYh29drvxTe5MKTL6Z6b2gU130_assertion
;
np:hasProvenance
dgn-np:NP938546.RA1Xkh9NTyd2xxSDJy5tZwYYh29drvxTe5MKTL6Z6b2gU130_provenance
;
np:hasPublicationInfo
dgn-np:NP938546.RA1Xkh9NTyd2xxSDJy5tZwYYh29drvxTe5MKTL6Z6b2gU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP938546.RA1Xkh9NTyd2xxSDJy5tZwYYh29drvxTe5MKTL6Z6b2gU130_assertion
a
np:Assertion
.
dgn-np:NP938546.RA1Xkh9NTyd2xxSDJy5tZwYYh29drvxTe5MKTL6Z6b2gU130_provenance
a
np:Provenance
.
dgn-np:NP938546.RA1Xkh9NTyd2xxSDJy5tZwYYh29drvxTe5MKTL6Z6b2gU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP938546.RA1Xkh9NTyd2xxSDJy5tZwYYh29drvxTe5MKTL6Z6b2gU130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0206681
a
ncit:C7057
.
dgn-gda:DGN077244f8fa91caebf3c68ab5e811aa20
sio:SIO_000628
miriam-gene:7157
,
lld:C0206681
;
a
sio:SIO_001121
.
}
dgn-np:NP938546.RA1Xkh9NTyd2xxSDJy5tZwYYh29drvxTe5MKTL6Z6b2gU130_provenance
{
dgn-np:NP938546.RA1Xkh9NTyd2xxSDJy5tZwYYh29drvxTe5MKTL6Z6b2gU130_assertion
dcterms:description
"[Loss of heterozygosity (LOH) in chromosome region 6q27 and p53 mutations were studied to attempt to clarify the genetic etiology of ovarian cancer, with particular reference to clear cell adenocarcinoma (CCC), which has a poor prognosis.]. 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:9789220
;
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:NP938546.RA1Xkh9NTyd2xxSDJy5tZwYYh29drvxTe5MKTL6Z6b2gU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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" .
}