@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP188839.RAQksssrlNS878ipd1opxefcNSgCpM_i-_OqDicAjYWlg
> .
@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:NP188839.RAQksssrlNS878ipd1opxefcNSgCpM_i-_OqDicAjYWlg130_head
{
this:
np:hasAssertion
dgn-np:NP188839.RAQksssrlNS878ipd1opxefcNSgCpM_i-_OqDicAjYWlg130_assertion
;
np:hasProvenance
dgn-np:NP188839.RAQksssrlNS878ipd1opxefcNSgCpM_i-_OqDicAjYWlg130_provenance
;
np:hasPublicationInfo
dgn-np:NP188839.RAQksssrlNS878ipd1opxefcNSgCpM_i-_OqDicAjYWlg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP188839.RAQksssrlNS878ipd1opxefcNSgCpM_i-_OqDicAjYWlg130_assertion
a
np:Assertion
.
dgn-np:NP188839.RAQksssrlNS878ipd1opxefcNSgCpM_i-_OqDicAjYWlg130_provenance
a
np:Provenance
.
dgn-np:NP188839.RAQksssrlNS878ipd1opxefcNSgCpM_i-_OqDicAjYWlg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP188839.RAQksssrlNS878ipd1opxefcNSgCpM_i-_OqDicAjYWlg130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0206681
a
ncit:C7057
.
dgn-gda:DGN6b3924b9036343312cda2d454313b939
sio:SIO_000628
miriam-gene:7157
,
lld:C0206681
;
a
sio:SIO_001121
.
}
dgn-np:NP188839.RAQksssrlNS878ipd1opxefcNSgCpM_i-_OqDicAjYWlg130_provenance
{
dgn-np:NP188839.RAQksssrlNS878ipd1opxefcNSgCpM_i-_OqDicAjYWlg130_assertion
dcterms:description
"[In addition, two cases of mixed serous and clear cell carcinoma showed an identical mutation of the p53 gene in the histologically distinct components and one case of mixed clear cell and endometrioid carcinoma had identical mutations in the PTEN and p53 genes, and microsatellite instability in both components.]. 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:14976538
;
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:NP188839.RAQksssrlNS878ipd1opxefcNSgCpM_i-_OqDicAjYWlg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:43+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" .
}