@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP529133.RAsU9slyoKWaHfRXWu1sK2Gl5jo6RCsN2Gp-1fUv3s3bE
> .
@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:NP529133.RAsU9slyoKWaHfRXWu1sK2Gl5jo6RCsN2Gp-1fUv3s3bE130_head
{
this:
np:hasAssertion
dgn-np:NP529133.RAsU9slyoKWaHfRXWu1sK2Gl5jo6RCsN2Gp-1fUv3s3bE130_assertion
;
np:hasProvenance
dgn-np:NP529133.RAsU9slyoKWaHfRXWu1sK2Gl5jo6RCsN2Gp-1fUv3s3bE130_provenance
;
np:hasPublicationInfo
dgn-np:NP529133.RAsU9slyoKWaHfRXWu1sK2Gl5jo6RCsN2Gp-1fUv3s3bE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP529133.RAsU9slyoKWaHfRXWu1sK2Gl5jo6RCsN2Gp-1fUv3s3bE130_assertion
a
np:Assertion
.
dgn-np:NP529133.RAsU9slyoKWaHfRXWu1sK2Gl5jo6RCsN2Gp-1fUv3s3bE130_provenance
a
np:Provenance
.
dgn-np:NP529133.RAsU9slyoKWaHfRXWu1sK2Gl5jo6RCsN2Gp-1fUv3s3bE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP529133.RAsU9slyoKWaHfRXWu1sK2Gl5jo6RCsN2Gp-1fUv3s3bE130_assertion
{
miriam-gene:6794
a
ncit:C16612
.
lld:C0001418
a
ncit:C7057
.
dgn-gda:DGN64b658cd894e07dc6eee44ebe7078fc0
sio:SIO_000628
miriam-gene:6794
,
lld:C0001418
;
a
sio:SIO_001121
.
}
dgn-np:NP529133.RAsU9slyoKWaHfRXWu1sK2Gl5jo6RCsN2Gp-1fUv3s3bE130_provenance
{
dgn-np:NP529133.RAsU9slyoKWaHfRXWu1sK2Gl5jo6RCsN2Gp-1fUv3s3bE130_assertion
dcterms:description
"[These results suggest that mutations in the STK11 gene may play an important role in the etiology of MDA of the uterine cervix and may distinguish this rare tumor from other common types of adenocarcinoma of the uterine cervix.]. 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:12533684
;
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:NP529133.RAsU9slyoKWaHfRXWu1sK2Gl5jo6RCsN2Gp-1fUv3s3bE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:19+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" .
}