@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP710414.RAPga-8P8Ve49LkhzMx4UBrFakKbNSmmLCnANb5S8bRF4
> .
@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:NP710414.RAPga-8P8Ve49LkhzMx4UBrFakKbNSmmLCnANb5S8bRF4130_head
{
this:
np:hasAssertion
dgn-np:NP710414.RAPga-8P8Ve49LkhzMx4UBrFakKbNSmmLCnANb5S8bRF4130_assertion
;
np:hasProvenance
dgn-np:NP710414.RAPga-8P8Ve49LkhzMx4UBrFakKbNSmmLCnANb5S8bRF4130_provenance
;
np:hasPublicationInfo
dgn-np:NP710414.RAPga-8P8Ve49LkhzMx4UBrFakKbNSmmLCnANb5S8bRF4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP710414.RAPga-8P8Ve49LkhzMx4UBrFakKbNSmmLCnANb5S8bRF4130_assertion
a
np:Assertion
.
dgn-np:NP710414.RAPga-8P8Ve49LkhzMx4UBrFakKbNSmmLCnANb5S8bRF4130_provenance
a
np:Provenance
.
dgn-np:NP710414.RAPga-8P8Ve49LkhzMx4UBrFakKbNSmmLCnANb5S8bRF4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP710414.RAPga-8P8Ve49LkhzMx4UBrFakKbNSmmLCnANb5S8bRF4130_assertion
{
miriam-gene:1728
a
ncit:C16612
.
lld:C1168401
a
ncit:C7057
.
dgn-gda:DGNd5838f1724e788cc27bd0248ab0e83e2
sio:SIO_000628
miriam-gene:1728
,
lld:C1168401
;
a
sio:SIO_001121
.
}
dgn-np:NP710414.RAPga-8P8Ve49LkhzMx4UBrFakKbNSmmLCnANb5S8bRF4130_provenance
{
dgn-np:NP710414.RAPga-8P8Ve49LkhzMx4UBrFakKbNSmmLCnANb5S8bRF4130_assertion
dcterms:description
"[A case: control study was carried out to determine if inactivating polymorphisms of the NQO1 gene at bases 609 and 465 are associated with altered risk of developing squamous cell carcinoma of the head and neck (SCCHN).]. 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:16054862
;
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:NP710414.RAPga-8P8Ve49LkhzMx4UBrFakKbNSmmLCnANb5S8bRF4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:12+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" .
}