@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP795933.RAmbQlgeKcLmo120e2d_rOza9eYFQ1NfAn_joBS_07hyQ
> .
@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:NP795933.RAmbQlgeKcLmo120e2d_rOza9eYFQ1NfAn_joBS_07hyQ130_head
{
this:
np:hasAssertion
dgn-np:NP795933.RAmbQlgeKcLmo120e2d_rOza9eYFQ1NfAn_joBS_07hyQ130_assertion
;
np:hasProvenance
dgn-np:NP795933.RAmbQlgeKcLmo120e2d_rOza9eYFQ1NfAn_joBS_07hyQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP795933.RAmbQlgeKcLmo120e2d_rOza9eYFQ1NfAn_joBS_07hyQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP795933.RAmbQlgeKcLmo120e2d_rOza9eYFQ1NfAn_joBS_07hyQ130_assertion
a
np:Assertion
.
dgn-np:NP795933.RAmbQlgeKcLmo120e2d_rOza9eYFQ1NfAn_joBS_07hyQ130_provenance
a
np:Provenance
.
dgn-np:NP795933.RAmbQlgeKcLmo120e2d_rOza9eYFQ1NfAn_joBS_07hyQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP795933.RAmbQlgeKcLmo120e2d_rOza9eYFQ1NfAn_joBS_07hyQ130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0032927
a
ncit:C7057
.
dgn-gda:DGN185877927109f7e98c284429d332f881
sio:SIO_000628
miriam-gene:5728
,
lld:C0032927
;
a
sio:SIO_001121
.
}
dgn-np:NP795933.RAmbQlgeKcLmo120e2d_rOza9eYFQ1NfAn_joBS_07hyQ130_provenance
{
dgn-np:NP795933.RAmbQlgeKcLmo120e2d_rOza9eYFQ1NfAn_joBS_07hyQ130_assertion
dcterms:description
"[Loss of PTEN function by mutational or other mechanisms is an early event in endometrial tumorigenesis that may occur in response to known endocrine risk factors and offers an informative immunohistochemical biomarker for premalignant disease.]. 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:10841828
;
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:NP795933.RAmbQlgeKcLmo120e2d_rOza9eYFQ1NfAn_joBS_07hyQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:08+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" .
}