@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP798584.RA9BhMERHd0pKOcBnWLa93x8JGeqMYvdkCbp6PoJXSQ_s
> .
@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:NP798584.RA9BhMERHd0pKOcBnWLa93x8JGeqMYvdkCbp6PoJXSQ_s130_head
{
this:
np:hasAssertion
dgn-np:NP798584.RA9BhMERHd0pKOcBnWLa93x8JGeqMYvdkCbp6PoJXSQ_s130_assertion
;
np:hasProvenance
dgn-np:NP798584.RA9BhMERHd0pKOcBnWLa93x8JGeqMYvdkCbp6PoJXSQ_s130_provenance
;
np:hasPublicationInfo
dgn-np:NP798584.RA9BhMERHd0pKOcBnWLa93x8JGeqMYvdkCbp6PoJXSQ_s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP798584.RA9BhMERHd0pKOcBnWLa93x8JGeqMYvdkCbp6PoJXSQ_s130_assertion
a
np:Assertion
.
dgn-np:NP798584.RA9BhMERHd0pKOcBnWLa93x8JGeqMYvdkCbp6PoJXSQ_s130_provenance
a
np:Provenance
.
dgn-np:NP798584.RA9BhMERHd0pKOcBnWLa93x8JGeqMYvdkCbp6PoJXSQ_s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP798584.RA9BhMERHd0pKOcBnWLa93x8JGeqMYvdkCbp6PoJXSQ_s130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0677886
a
ncit:C7057
.
dgn-gda:DGN006173d967088cc78bee379eec9fff50
sio:SIO_000628
miriam-gene:7248
,
lld:C0677886
;
a
sio:SIO_001121
.
}
dgn-np:NP798584.RA9BhMERHd0pKOcBnWLa93x8JGeqMYvdkCbp6PoJXSQ_s130_provenance
{
dgn-np:NP798584.RA9BhMERHd0pKOcBnWLa93x8JGeqMYvdkCbp6PoJXSQ_s130_assertion
dcterms:description
"[Evidence of mutations in the tumour suppressor PTEN gene in the endometrioid subtype of epithelial ovarian cancer further suggests that somatic genetic alterations represent early events in the transformation of benign endometriotic cells.]. 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:10711828
;
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:NP798584.RA9BhMERHd0pKOcBnWLa93x8JGeqMYvdkCbp6PoJXSQ_s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:10+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" .
}