@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP625488.RA_-yrm68DutAeliEhQ6cGq9H2qGUTJHj2qDTmHEFNdfw
> .
@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:NP625488.RA_-yrm68DutAeliEhQ6cGq9H2qGUTJHj2qDTmHEFNdfw130_head
{
this:
np:hasAssertion
dgn-np:NP625488.RA_-yrm68DutAeliEhQ6cGq9H2qGUTJHj2qDTmHEFNdfw130_assertion
;
np:hasProvenance
dgn-np:NP625488.RA_-yrm68DutAeliEhQ6cGq9H2qGUTJHj2qDTmHEFNdfw130_provenance
;
np:hasPublicationInfo
dgn-np:NP625488.RA_-yrm68DutAeliEhQ6cGq9H2qGUTJHj2qDTmHEFNdfw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP625488.RA_-yrm68DutAeliEhQ6cGq9H2qGUTJHj2qDTmHEFNdfw130_assertion
a
np:Assertion
.
dgn-np:NP625488.RA_-yrm68DutAeliEhQ6cGq9H2qGUTJHj2qDTmHEFNdfw130_provenance
a
np:Provenance
.
dgn-np:NP625488.RA_-yrm68DutAeliEhQ6cGq9H2qGUTJHj2qDTmHEFNdfw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP625488.RA_-yrm68DutAeliEhQ6cGq9H2qGUTJHj2qDTmHEFNdfw130_assertion
{
miriam-gene:83478
a
ncit:C16612
.
lld:C0007121
a
ncit:C7057
.
dgn-gda:DGNcc9c0e65a67160ad44f692548fd55314
sio:SIO_000628
miriam-gene:83478
,
lld:C0007121
;
a
sio:SIO_001121
.
}
dgn-np:NP625488.RA_-yrm68DutAeliEhQ6cGq9H2qGUTJHj2qDTmHEFNdfw130_provenance
{
dgn-np:NP625488.RA_-yrm68DutAeliEhQ6cGq9H2qGUTJHj2qDTmHEFNdfw130_assertion
dcterms:description
"[p21 TA levels vary considerably among BC patients which may be attributable to 1) genetic alterations in Rb and p53 and 2) variation in TA levels of upstream transcription factors E2F1 and p73.]. 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:16014176
;
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:NP625488.RA_-yrm68DutAeliEhQ6cGq9H2qGUTJHj2qDTmHEFNdfw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:17+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" .
}