@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP653656.RAdi0NqN88SmUgTcWITwEg0psuVFiocnqxr0Q7Gq8C2bY
> .
@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:NP653656.RAdi0NqN88SmUgTcWITwEg0psuVFiocnqxr0Q7Gq8C2bY130_head
{
this:
np:hasAssertion
dgn-np:NP653656.RAdi0NqN88SmUgTcWITwEg0psuVFiocnqxr0Q7Gq8C2bY130_assertion
;
np:hasProvenance
dgn-np:NP653656.RAdi0NqN88SmUgTcWITwEg0psuVFiocnqxr0Q7Gq8C2bY130_provenance
;
np:hasPublicationInfo
dgn-np:NP653656.RAdi0NqN88SmUgTcWITwEg0psuVFiocnqxr0Q7Gq8C2bY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP653656.RAdi0NqN88SmUgTcWITwEg0psuVFiocnqxr0Q7Gq8C2bY130_assertion
a
np:Assertion
.
dgn-np:NP653656.RAdi0NqN88SmUgTcWITwEg0psuVFiocnqxr0Q7Gq8C2bY130_provenance
a
np:Provenance
.
dgn-np:NP653656.RAdi0NqN88SmUgTcWITwEg0psuVFiocnqxr0Q7Gq8C2bY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP653656.RAdi0NqN88SmUgTcWITwEg0psuVFiocnqxr0Q7Gq8C2bY130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0029925
a
ncit:C7057
.
dgn-gda:DGNf0d97328002113e2f8d9109f14994bac
sio:SIO_000628
miriam-gene:3342
,
lld:C0029925
;
a
sio:SIO_001121
.
}
dgn-np:NP653656.RAdi0NqN88SmUgTcWITwEg0psuVFiocnqxr0Q7Gq8C2bY130_provenance
{
dgn-np:NP653656.RAdi0NqN88SmUgTcWITwEg0psuVFiocnqxr0Q7Gq8C2bY130_assertion
dcterms:description
"[Our results imply that the major gross genetic changes in ovarian cancer take place in the primary tumor, and the additional genetic changes that may occur in the metastases are not detectable by CGH.]. 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:15381367
;
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:NP653656.RAdi0NqN88SmUgTcWITwEg0psuVFiocnqxr0Q7Gq8C2bY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:33+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" .
}