@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP846910.RArlOQDwb83_fUbKYTeNbICtKwweVUWfUpb6YZ770lWKg
> .
@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:NP846910.RArlOQDwb83_fUbKYTeNbICtKwweVUWfUpb6YZ770lWKg130_head
{
this:
np:hasAssertion
dgn-np:NP846910.RArlOQDwb83_fUbKYTeNbICtKwweVUWfUpb6YZ770lWKg130_assertion
;
np:hasProvenance
dgn-np:NP846910.RArlOQDwb83_fUbKYTeNbICtKwweVUWfUpb6YZ770lWKg130_provenance
;
np:hasPublicationInfo
dgn-np:NP846910.RArlOQDwb83_fUbKYTeNbICtKwweVUWfUpb6YZ770lWKg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP846910.RArlOQDwb83_fUbKYTeNbICtKwweVUWfUpb6YZ770lWKg130_assertion
a
np:Assertion
.
dgn-np:NP846910.RArlOQDwb83_fUbKYTeNbICtKwweVUWfUpb6YZ770lWKg130_provenance
a
np:Provenance
.
dgn-np:NP846910.RArlOQDwb83_fUbKYTeNbICtKwweVUWfUpb6YZ770lWKg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP846910.RArlOQDwb83_fUbKYTeNbICtKwweVUWfUpb6YZ770lWKg130_assertion
{
miriam-gene:5290
a
ncit:C16612
.
lld:C0206681
a
ncit:C7057
.
dgn-gda:DGNbb8f7b8d092f946c0093eb2387a8b67e
sio:SIO_000628
miriam-gene:5290
,
lld:C0206681
;
a
sio:SIO_001121
.
}
dgn-np:NP846910.RArlOQDwb83_fUbKYTeNbICtKwweVUWfUpb6YZ770lWKg130_provenance
{
dgn-np:NP846910.RArlOQDwb83_fUbKYTeNbICtKwweVUWfUpb6YZ770lWKg130_assertion
dcterms:description
"[In the last few years, mutations in ARID1A and PIK3CA have been described in a substantial fraction of cases of ovarian clear cell carcinoma, yet the paper by Yamamoto et al in this issue of The Journal of Pathology reveals that PIK3CA mutations can be detected in precursor endometriosis tissues.]. 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:21898874
;
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:NP846910.RArlOQDwb83_fUbKYTeNbICtKwweVUWfUpb6YZ770lWKg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:37+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" .
}