@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP586992.RAQ0mCXhJNtAiE_sWBFROds-xbQmaY2eOlgU2Qsar398s
> .
@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:NP586992.RAQ0mCXhJNtAiE_sWBFROds-xbQmaY2eOlgU2Qsar398s130_head
{
this:
np:hasAssertion
dgn-np:NP586992.RAQ0mCXhJNtAiE_sWBFROds-xbQmaY2eOlgU2Qsar398s130_assertion
;
np:hasProvenance
dgn-np:NP586992.RAQ0mCXhJNtAiE_sWBFROds-xbQmaY2eOlgU2Qsar398s130_provenance
;
np:hasPublicationInfo
dgn-np:NP586992.RAQ0mCXhJNtAiE_sWBFROds-xbQmaY2eOlgU2Qsar398s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP586992.RAQ0mCXhJNtAiE_sWBFROds-xbQmaY2eOlgU2Qsar398s130_assertion
a
np:Assertion
.
dgn-np:NP586992.RAQ0mCXhJNtAiE_sWBFROds-xbQmaY2eOlgU2Qsar398s130_provenance
a
np:Provenance
.
dgn-np:NP586992.RAQ0mCXhJNtAiE_sWBFROds-xbQmaY2eOlgU2Qsar398s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP586992.RAQ0mCXhJNtAiE_sWBFROds-xbQmaY2eOlgU2Qsar398s130_assertion
{
miriam-gene:133482
a
ncit:C16612
.
lld:C0023531
a
ncit:C7057
.
dgn-gda:DGN5d3aafca390664ef2ec231a6cb754b63
sio:SIO_000628
miriam-gene:133482
,
lld:C0023531
;
a
sio:SIO_001121
.
}
dgn-np:NP586992.RAQ0mCXhJNtAiE_sWBFROds-xbQmaY2eOlgU2Qsar398s130_provenance
{
dgn-np:NP586992.RAQ0mCXhJNtAiE_sWBFROds-xbQmaY2eOlgU2Qsar398s130_assertion
dcterms:description
"[Here the mtDNA polymorphisms at 12,308 nucleotide pairs (np), 11,467 np, 10,400 np, and 10,398 np were studied to examine the association with the risk of oral cancer and leukoplakia, alone and in combination with polymorphisms at the GST loci.]. 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:17886251
;
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:NP586992.RAQ0mCXhJNtAiE_sWBFROds-xbQmaY2eOlgU2Qsar398s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:53+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" .
}