@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44968.RAKhzQ5pn7651bCFHHuOg_ZHJeIFBODCZJDArUpvVt1rg
> .
@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:NP44968.RAKhzQ5pn7651bCFHHuOg_ZHJeIFBODCZJDArUpvVt1rg130_head
{
this:
np:hasAssertion
dgn-np:NP44968.RAKhzQ5pn7651bCFHHuOg_ZHJeIFBODCZJDArUpvVt1rg130_assertion
;
np:hasProvenance
dgn-np:NP44968.RAKhzQ5pn7651bCFHHuOg_ZHJeIFBODCZJDArUpvVt1rg130_provenance
;
np:hasPublicationInfo
dgn-np:NP44968.RAKhzQ5pn7651bCFHHuOg_ZHJeIFBODCZJDArUpvVt1rg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44968.RAKhzQ5pn7651bCFHHuOg_ZHJeIFBODCZJDArUpvVt1rg130_assertion
a
np:Assertion
.
dgn-np:NP44968.RAKhzQ5pn7651bCFHHuOg_ZHJeIFBODCZJDArUpvVt1rg130_provenance
a
np:Provenance
.
dgn-np:NP44968.RAKhzQ5pn7651bCFHHuOg_ZHJeIFBODCZJDArUpvVt1rg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44968.RAKhzQ5pn7651bCFHHuOg_ZHJeIFBODCZJDArUpvVt1rg130_assertion
{
miriam-gene:2067
a
ncit:C16612
.
lld:C0278996
a
ncit:C7057
.
dgn-gda:DGN933525ff4d2d986fde9cff5acb13dfa5
sio:SIO_000628
miriam-gene:2067
,
lld:C0278996
;
a
sio:SIO_001122
.
}
dgn-np:NP44968.RAKhzQ5pn7651bCFHHuOg_ZHJeIFBODCZJDArUpvVt1rg130_provenance
{
dgn-np:NP44968.RAKhzQ5pn7651bCFHHuOg_ZHJeIFBODCZJDArUpvVt1rg130_assertion
dcterms:description
"[ These 2 polymorphisms may contribute to the risk of SCCHN, but larger studies are needed to confirm their role in SCCHN. Combining common DNA repair gene polymorphisms into models of genetic risk of SCCHN may improve risk estimates.]. 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:12220217
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP44968.RAKhzQ5pn7651bCFHHuOg_ZHJeIFBODCZJDArUpvVt1rg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}