@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP410169.RAYmMXWFDa3BFokRRkJ3d7c0ExYOYRtLV0rrN9GjFyjwc
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP410169.RAYmMXWFDa3BFokRRkJ3d7c0ExYOYRtLV0rrN9GjFyjwc130_head
{
this:
np:hasAssertion
dgn-np:NP410169.RAYmMXWFDa3BFokRRkJ3d7c0ExYOYRtLV0rrN9GjFyjwc130_assertion
;
np:hasProvenance
dgn-np:NP410169.RAYmMXWFDa3BFokRRkJ3d7c0ExYOYRtLV0rrN9GjFyjwc130_provenance
;
np:hasPublicationInfo
dgn-np:NP410169.RAYmMXWFDa3BFokRRkJ3d7c0ExYOYRtLV0rrN9GjFyjwc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP410169.RAYmMXWFDa3BFokRRkJ3d7c0ExYOYRtLV0rrN9GjFyjwc130_assertion
a
np:Assertion
.
dgn-np:NP410169.RAYmMXWFDa3BFokRRkJ3d7c0ExYOYRtLV0rrN9GjFyjwc130_provenance
a
np:Provenance
.
dgn-np:NP410169.RAYmMXWFDa3BFokRRkJ3d7c0ExYOYRtLV0rrN9GjFyjwc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP410169.RAYmMXWFDa3BFokRRkJ3d7c0ExYOYRtLV0rrN9GjFyjwc130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGNd6636338bb6daa444c6a1a6148de7e03
sio:SIO_000628
miriam-gene:7157
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP410169.RAYmMXWFDa3BFokRRkJ3d7c0ExYOYRtLV0rrN9GjFyjwc130_provenance
{
dgn-np:NP410169.RAYmMXWFDa3BFokRRkJ3d7c0ExYOYRtLV0rrN9GjFyjwc130_assertion
dcterms:description
"[Therefore, p53 gene mutation is suggested to occur independently of the type of viral infection or status of preexisting liver disease and to occur preferentially in moderately and poorly differentiated HCCs in association with or after loss of another p53 allele as a late event of HCC progression.]. 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:1330291
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP410169.RAYmMXWFDa3BFokRRkJ3d7c0ExYOYRtLV0rrN9GjFyjwc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:51+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}