@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP847472.RAbutGOuXnZNo1H998XbvR3yVvrB4B0MFY2alQO5PPdco
> .
@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:NP847472.RAbutGOuXnZNo1H998XbvR3yVvrB4B0MFY2alQO5PPdco130_head
{
this:
np:hasAssertion
dgn-np:NP847472.RAbutGOuXnZNo1H998XbvR3yVvrB4B0MFY2alQO5PPdco130_assertion
;
np:hasProvenance
dgn-np:NP847472.RAbutGOuXnZNo1H998XbvR3yVvrB4B0MFY2alQO5PPdco130_provenance
;
np:hasPublicationInfo
dgn-np:NP847472.RAbutGOuXnZNo1H998XbvR3yVvrB4B0MFY2alQO5PPdco130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP847472.RAbutGOuXnZNo1H998XbvR3yVvrB4B0MFY2alQO5PPdco130_assertion
a
np:Assertion
.
dgn-np:NP847472.RAbutGOuXnZNo1H998XbvR3yVvrB4B0MFY2alQO5PPdco130_provenance
a
np:Provenance
.
dgn-np:NP847472.RAbutGOuXnZNo1H998XbvR3yVvrB4B0MFY2alQO5PPdco130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP847472.RAbutGOuXnZNo1H998XbvR3yVvrB4B0MFY2alQO5PPdco130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0280631
a
ncit:C7057
.
dgn-gda:DGN6a5f6a2eb66a596c24b3a9695a4bad3e
sio:SIO_000628
miriam-gene:7157
,
lld:C0280631
;
a
sio:SIO_001121
.
}
dgn-np:NP847472.RAbutGOuXnZNo1H998XbvR3yVvrB4B0MFY2alQO5PPdco130_provenance
{
dgn-np:NP847472.RAbutGOuXnZNo1H998XbvR3yVvrB4B0MFY2alQO5PPdco130_assertion
dcterms:description
"[We showed that conditional deletion of p53 in mice results in the development of uterine tumors that resemble human ULMS and that concurrent deletion of p53 and BRCA1 significantly accelerates the progression of these tumors.]. 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:19843854
;
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:NP847472.RAbutGOuXnZNo1H998XbvR3yVvrB4B0MFY2alQO5PPdco130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:38+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" .
}