@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE
> .
@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:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_head
{
this:
np:hasAssertion
dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_assertion
;
np:hasProvenance
dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_provenance
;
np:hasPublicationInfo
dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_assertion
a
np:Assertion
.
dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_provenance
a
np:Provenance
.
dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_assertion
{
miriam-gene:5888
a
ncit:C16612
.
lld:C2239176
a
ncit:C7057
.
dgn-gda:DGN5bd5c4fc4456373004c20d386fbf2930
sio:SIO_000628
miriam-gene:5888
,
lld:C2239176
;
a
sio:SIO_001121
.
}
dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_provenance
{
dgn-np:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_assertion
dcterms:description
"[Furthermore, with age of infection as an important factor in disease progression to HCC, results from the Cox proportional hazards analysis showed no significant associations between any of the tested RAD51 variants and the age of onset of HCC (P > 0.05), suggesting that genetic polymorphisms of RAD51 may not play an important role in clearance of HBV and disease progression to 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:21915862
;
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:NP767924.RAsvDOsAMeIDGfB_0ypnUTjJociFdYqzmVe_G9nEnaKtE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:44+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" .
}