@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP453089.RAayGvqgetUBaLvtKW6NNVyL95QyrsnymO9KSSkY2Qilc
> .
@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:NP453089.RAayGvqgetUBaLvtKW6NNVyL95QyrsnymO9KSSkY2Qilc130_head
{
this:
np:hasAssertion
dgn-np:NP453089.RAayGvqgetUBaLvtKW6NNVyL95QyrsnymO9KSSkY2Qilc130_assertion
;
np:hasProvenance
dgn-np:NP453089.RAayGvqgetUBaLvtKW6NNVyL95QyrsnymO9KSSkY2Qilc130_provenance
;
np:hasPublicationInfo
dgn-np:NP453089.RAayGvqgetUBaLvtKW6NNVyL95QyrsnymO9KSSkY2Qilc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP453089.RAayGvqgetUBaLvtKW6NNVyL95QyrsnymO9KSSkY2Qilc130_assertion
a
np:Assertion
.
dgn-np:NP453089.RAayGvqgetUBaLvtKW6NNVyL95QyrsnymO9KSSkY2Qilc130_provenance
a
np:Provenance
.
dgn-np:NP453089.RAayGvqgetUBaLvtKW6NNVyL95QyrsnymO9KSSkY2Qilc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP453089.RAayGvqgetUBaLvtKW6NNVyL95QyrsnymO9KSSkY2Qilc130_assertion
{
miriam-gene:208
a
ncit:C16612
.
lld:C0029925
a
ncit:C7057
.
dgn-gda:DGNc606e71fb6ecc18302546c7d5bb1ddbe
sio:SIO_000628
miriam-gene:208
,
lld:C0029925
;
a
sio:SIO_001121
.
}
dgn-np:NP453089.RAayGvqgetUBaLvtKW6NNVyL95QyrsnymO9KSSkY2Qilc130_provenance
{
dgn-np:NP453089.RAayGvqgetUBaLvtKW6NNVyL95QyrsnymO9KSSkY2Qilc130_assertion
dcterms:description
"[Because amplification of AKT2 putative oncogene has been detected in ovarian carcinomas bearing HSR and in this case NHL, we believe that this gene may be implicated in the pathogenesis of other neoplasias in cooperation with other genes.]. 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:8646732
;
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:NP453089.RAayGvqgetUBaLvtKW6NNVyL95QyrsnymO9KSSkY2Qilc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:30+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" .
}