@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP448362.RA5soOmSGrI__Bi9j6iyy29YQyFg9xZ5m6Ot1DmIjhKpU
> .
@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:NP448362.RA5soOmSGrI__Bi9j6iyy29YQyFg9xZ5m6Ot1DmIjhKpU130_head
{
this:
np:hasAssertion
dgn-np:NP448362.RA5soOmSGrI__Bi9j6iyy29YQyFg9xZ5m6Ot1DmIjhKpU130_assertion
;
np:hasProvenance
dgn-np:NP448362.RA5soOmSGrI__Bi9j6iyy29YQyFg9xZ5m6Ot1DmIjhKpU130_provenance
;
np:hasPublicationInfo
dgn-np:NP448362.RA5soOmSGrI__Bi9j6iyy29YQyFg9xZ5m6Ot1DmIjhKpU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP448362.RA5soOmSGrI__Bi9j6iyy29YQyFg9xZ5m6Ot1DmIjhKpU130_assertion
a
np:Assertion
.
dgn-np:NP448362.RA5soOmSGrI__Bi9j6iyy29YQyFg9xZ5m6Ot1DmIjhKpU130_provenance
a
np:Provenance
.
dgn-np:NP448362.RA5soOmSGrI__Bi9j6iyy29YQyFg9xZ5m6Ot1DmIjhKpU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP448362.RA5soOmSGrI__Bi9j6iyy29YQyFg9xZ5m6Ot1DmIjhKpU130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0019159
a
ncit:C7057
.
dgn-gda:DGN44b30205217cf17ad1877d7bf3591b72
sio:SIO_000628
miriam-gene:7157
,
lld:C0019159
;
a
sio:SIO_001121
.
}
dgn-np:NP448362.RA5soOmSGrI__Bi9j6iyy29YQyFg9xZ5m6Ot1DmIjhKpU130_provenance
{
dgn-np:NP448362.RA5soOmSGrI__Bi9j6iyy29YQyFg9xZ5m6Ot1DmIjhKpU130_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:NP448362.RA5soOmSGrI__Bi9j6iyy29YQyFg9xZ5m6Ot1DmIjhKpU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:27+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" .
}