@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP900386.RA3VW0IpOmYJG27FQyq8brDNvPb7ui8T227PxG3zEg1kA
> .
@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:NP900386.RA3VW0IpOmYJG27FQyq8brDNvPb7ui8T227PxG3zEg1kA130_head
{
this:
np:hasAssertion
dgn-np:NP900386.RA3VW0IpOmYJG27FQyq8brDNvPb7ui8T227PxG3zEg1kA130_assertion
;
np:hasProvenance
dgn-np:NP900386.RA3VW0IpOmYJG27FQyq8brDNvPb7ui8T227PxG3zEg1kA130_provenance
;
np:hasPublicationInfo
dgn-np:NP900386.RA3VW0IpOmYJG27FQyq8brDNvPb7ui8T227PxG3zEg1kA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP900386.RA3VW0IpOmYJG27FQyq8brDNvPb7ui8T227PxG3zEg1kA130_assertion
a
np:Assertion
.
dgn-np:NP900386.RA3VW0IpOmYJG27FQyq8brDNvPb7ui8T227PxG3zEg1kA130_provenance
a
np:Provenance
.
dgn-np:NP900386.RA3VW0IpOmYJG27FQyq8brDNvPb7ui8T227PxG3zEg1kA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP900386.RA3VW0IpOmYJG27FQyq8brDNvPb7ui8T227PxG3zEg1kA130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0019158
a
ncit:C7057
.
dgn-gda:DGNd54b0893dfa686b1141a43e3ef4d9d53
sio:SIO_000628
miriam-gene:7157
,
lld:C0019158
;
a
sio:SIO_001121
.
}
dgn-np:NP900386.RA3VW0IpOmYJG27FQyq8brDNvPb7ui8T227PxG3zEg1kA130_provenance
{
dgn-np:NP900386.RA3VW0IpOmYJG27FQyq8brDNvPb7ui8T227PxG3zEg1kA130_assertion
dcterms:description
"[The incidence of p53 gene abnormalities in human hepatocellular carcinoma (HCC) varies in different geographical areas, being higher in regions where hepatitis virus infection and dietary exposure to aflatoxin B1 are the most common aetiological agents.]. 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:10394883
;
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:NP900386.RA3VW0IpOmYJG27FQyq8brDNvPb7ui8T227PxG3zEg1kA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:13+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" .
}