@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP486006.RAwqze1CQJZsTVHX32dGXQOUnCNLMhxuLufsEXXinPccw
> .
@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:NP486006.RAwqze1CQJZsTVHX32dGXQOUnCNLMhxuLufsEXXinPccw130_head
{
this:
np:hasAssertion
dgn-np:NP486006.RAwqze1CQJZsTVHX32dGXQOUnCNLMhxuLufsEXXinPccw130_assertion
;
np:hasProvenance
dgn-np:NP486006.RAwqze1CQJZsTVHX32dGXQOUnCNLMhxuLufsEXXinPccw130_provenance
;
np:hasPublicationInfo
dgn-np:NP486006.RAwqze1CQJZsTVHX32dGXQOUnCNLMhxuLufsEXXinPccw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP486006.RAwqze1CQJZsTVHX32dGXQOUnCNLMhxuLufsEXXinPccw130_assertion
a
np:Assertion
.
dgn-np:NP486006.RAwqze1CQJZsTVHX32dGXQOUnCNLMhxuLufsEXXinPccw130_provenance
a
np:Provenance
.
dgn-np:NP486006.RAwqze1CQJZsTVHX32dGXQOUnCNLMhxuLufsEXXinPccw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP486006.RAwqze1CQJZsTVHX32dGXQOUnCNLMhxuLufsEXXinPccw130_assertion
{
miriam-gene:1950
a
ncit:C16612
.
lld:C0023890
a
ncit:C7057
.
dgn-gda:DGN725c09a12a21ffbc76b19bea24d98aae
sio:SIO_000628
miriam-gene:1950
,
lld:C0023890
;
a
sio:SIO_001121
.
}
dgn-np:NP486006.RAwqze1CQJZsTVHX32dGXQOUnCNLMhxuLufsEXXinPccw130_provenance
{
dgn-np:NP486006.RAwqze1CQJZsTVHX32dGXQOUnCNLMhxuLufsEXXinPccw130_assertion
dcterms:description
"[The present results show that although EGF gene A61G polymorphism is associated with development of HCC in liver cirrhosis, it is not sufficient for HCC in Chinese patients with chronic HBV infection.]. 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:19900104
;
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:NP486006.RAwqze1CQJZsTVHX32dGXQOUnCNLMhxuLufsEXXinPccw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:50+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" .
}