@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ
> .
@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:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_head
{
this:
np:hasAssertion
dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_assertion
;
np:hasProvenance
dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_assertion
a
np:Assertion
.
dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_provenance
a
np:Provenance
.
dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C1332347
a
ncit:C7057
.
dgn-gda:DGN5dc344605200c2c07fd26371d476db45
sio:SIO_000628
miriam-gene:7157
,
lld:C1332347
;
a
sio:SIO_001121
.
}
dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_provenance
{
dgn-np:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_assertion
dcterms:description
"[The aims of this study were to determine the status and timing of p53 mutation in the progression from atypical ductal hyperplasia to invasive cancer, and to evaluate the patterns of p53 mutations in noninvasive and invasive lesions.]. 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:11715068
;
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:NP663186.RA_3AfGXZ-972fkG5yGxtVsSG-MBb3yS7SqjYG7WATAoQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:40+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" .
}