@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP628016.RATgSk2qhZK4rrMrwSABSu1TKrvgkeHPfCnMysmv86D0M
> .
@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:NP628016.RATgSk2qhZK4rrMrwSABSu1TKrvgkeHPfCnMysmv86D0M130_head
{
this:
np:hasAssertion
dgn-np:NP628016.RATgSk2qhZK4rrMrwSABSu1TKrvgkeHPfCnMysmv86D0M130_assertion
;
np:hasProvenance
dgn-np:NP628016.RATgSk2qhZK4rrMrwSABSu1TKrvgkeHPfCnMysmv86D0M130_provenance
;
np:hasPublicationInfo
dgn-np:NP628016.RATgSk2qhZK4rrMrwSABSu1TKrvgkeHPfCnMysmv86D0M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP628016.RATgSk2qhZK4rrMrwSABSu1TKrvgkeHPfCnMysmv86D0M130_assertion
a
np:Assertion
.
dgn-np:NP628016.RATgSk2qhZK4rrMrwSABSu1TKrvgkeHPfCnMysmv86D0M130_provenance
a
np:Provenance
.
dgn-np:NP628016.RATgSk2qhZK4rrMrwSABSu1TKrvgkeHPfCnMysmv86D0M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP628016.RATgSk2qhZK4rrMrwSABSu1TKrvgkeHPfCnMysmv86D0M130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0013930
a
ncit:C7057
.
dgn-gda:DGN0ed12abf294e0e11bca81196425eb21b
sio:SIO_000628
miriam-gene:7157
,
lld:C0013930
;
a
sio:SIO_001121
.
}
dgn-np:NP628016.RATgSk2qhZK4rrMrwSABSu1TKrvgkeHPfCnMysmv86D0M130_provenance
{
dgn-np:NP628016.RATgSk2qhZK4rrMrwSABSu1TKrvgkeHPfCnMysmv86D0M130_assertion
dcterms:description
"[There was a positive association of expression levels of both P3 and P4 transcripts in HCC tissues with the p53 mutation and presence of tumor embolus of portal vein, and expression of P3 were negatively related to differentiation of HCC.]. 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:16697535
;
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:NP628016.RATgSk2qhZK4rrMrwSABSu1TKrvgkeHPfCnMysmv86D0M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:19+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" .
}