@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP720588.RAmzvGE9mW0zUEi815mDxuS19_Fk1SfqzDAB3dsObSDTw
> .
@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:NP720588.RAmzvGE9mW0zUEi815mDxuS19_Fk1SfqzDAB3dsObSDTw130_head
{
this:
np:hasAssertion
dgn-np:NP720588.RAmzvGE9mW0zUEi815mDxuS19_Fk1SfqzDAB3dsObSDTw130_assertion
;
np:hasProvenance
dgn-np:NP720588.RAmzvGE9mW0zUEi815mDxuS19_Fk1SfqzDAB3dsObSDTw130_provenance
;
np:hasPublicationInfo
dgn-np:NP720588.RAmzvGE9mW0zUEi815mDxuS19_Fk1SfqzDAB3dsObSDTw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP720588.RAmzvGE9mW0zUEi815mDxuS19_Fk1SfqzDAB3dsObSDTw130_assertion
a
np:Assertion
.
dgn-np:NP720588.RAmzvGE9mW0zUEi815mDxuS19_Fk1SfqzDAB3dsObSDTw130_provenance
a
np:Provenance
.
dgn-np:NP720588.RAmzvGE9mW0zUEi815mDxuS19_Fk1SfqzDAB3dsObSDTw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP720588.RAmzvGE9mW0zUEi815mDxuS19_Fk1SfqzDAB3dsObSDTw130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0016034
a
ncit:C7057
.
dgn-gda:DGNe33d0b6c780766342d03da94cc0631b3
sio:SIO_000628
miriam-gene:7157
,
lld:C0016034
;
a
sio:SIO_001121
.
}
dgn-np:NP720588.RAmzvGE9mW0zUEi815mDxuS19_Fk1SfqzDAB3dsObSDTw130_provenance
{
dgn-np:NP720588.RAmzvGE9mW0zUEi815mDxuS19_Fk1SfqzDAB3dsObSDTw130_assertion
dcterms:description
"[The results of this study suggest that p53 protein accumulation and nonpolymorphic intronic changes in p53 are associated with increased risk of progression to breast cancer in women with benign breast disease.]. 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:16835330
;
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:NP720588.RAmzvGE9mW0zUEi815mDxuS19_Fk1SfqzDAB3dsObSDTw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:17+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" .
}