@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP535493.RASW_AiPVVjlWjfewXrttMOsvQw9QCEvh1DebMQyI1GBU
> .
@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:NP535493.RASW_AiPVVjlWjfewXrttMOsvQw9QCEvh1DebMQyI1GBU130_head
{
this:
np:hasAssertion
dgn-np:NP535493.RASW_AiPVVjlWjfewXrttMOsvQw9QCEvh1DebMQyI1GBU130_assertion
;
np:hasProvenance
dgn-np:NP535493.RASW_AiPVVjlWjfewXrttMOsvQw9QCEvh1DebMQyI1GBU130_provenance
;
np:hasPublicationInfo
dgn-np:NP535493.RASW_AiPVVjlWjfewXrttMOsvQw9QCEvh1DebMQyI1GBU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP535493.RASW_AiPVVjlWjfewXrttMOsvQw9QCEvh1DebMQyI1GBU130_assertion
a
np:Assertion
.
dgn-np:NP535493.RASW_AiPVVjlWjfewXrttMOsvQw9QCEvh1DebMQyI1GBU130_provenance
a
np:Provenance
.
dgn-np:NP535493.RASW_AiPVVjlWjfewXrttMOsvQw9QCEvh1DebMQyI1GBU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP535493.RASW_AiPVVjlWjfewXrttMOsvQw9QCEvh1DebMQyI1GBU130_assertion
{
miriam-gene:3451
a
ncit:C16612
.
lld:C0279671
a
ncit:C7057
.
dgn-gda:DGN2f54d1bda435e9ff096165c7e9e7075c
sio:SIO_000628
miriam-gene:3451
,
lld:C0279671
;
a
sio:SIO_001121
.
}
dgn-np:NP535493.RASW_AiPVVjlWjfewXrttMOsvQw9QCEvh1DebMQyI1GBU130_provenance
{
dgn-np:NP535493.RASW_AiPVVjlWjfewXrttMOsvQw9QCEvh1DebMQyI1GBU130_assertion
dcterms:description
"[The aim of this study was to estimate whether the Ile184Arg polymorphism of the Interferon, alpha 17 (IFNA17) gene might be correlated with the risk and prognosis of cervical squamous cell carcinoma (SCCA).]. 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:12490311
;
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:NP535493.RASW_AiPVVjlWjfewXrttMOsvQw9QCEvh1DebMQyI1GBU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:23+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
> , <
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> , <
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" .
}