@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg
> .
@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:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_head
{
this:
np:hasAssertion
dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_assertion
;
np:hasProvenance
dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_provenance
;
np:hasPublicationInfo
dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_assertion
a
np:Assertion
.
dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_provenance
a
np:Provenance
.
dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_assertion
{
miriam-gene:8170
a
ncit:C16612
.
lld:C0019163
a
ncit:C7057
.
dgn-gda:DGN5f97ae4beff7212b09399a8cf7e50942
sio:SIO_000628
miriam-gene:8170
,
lld:C0019163
;
a
sio:SIO_001121
.
}
dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_provenance
{
dgn-np:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_assertion
dcterms:description
"[The associations between seven common GRP78 polymorphisms in the promoter (rs391957, rs17840762, rs17840761, rs11355458) and in the 3' untranslated region (UTR) (rs16927997, rs1140763, rs12009) and possible risk of chronic HBV infection were assessed in a case-control study.]. 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:20525207
;
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:NP523675.RAhJYBGOyob7Pe3g77No5EqTk6jDHZ0PuyrbvCmIqpXbg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:14+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" .
}