@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP387580.RA8GLOETG7mvZvhxqCH_E7wPgfJ0C9D91zcoTcm_6OCUk
> .
@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:NP387580.RA8GLOETG7mvZvhxqCH_E7wPgfJ0C9D91zcoTcm_6OCUk130_head
{
this:
np:hasAssertion
dgn-np:NP387580.RA8GLOETG7mvZvhxqCH_E7wPgfJ0C9D91zcoTcm_6OCUk130_assertion
;
np:hasProvenance
dgn-np:NP387580.RA8GLOETG7mvZvhxqCH_E7wPgfJ0C9D91zcoTcm_6OCUk130_provenance
;
np:hasPublicationInfo
dgn-np:NP387580.RA8GLOETG7mvZvhxqCH_E7wPgfJ0C9D91zcoTcm_6OCUk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP387580.RA8GLOETG7mvZvhxqCH_E7wPgfJ0C9D91zcoTcm_6OCUk130_assertion
a
np:Assertion
.
dgn-np:NP387580.RA8GLOETG7mvZvhxqCH_E7wPgfJ0C9D91zcoTcm_6OCUk130_provenance
a
np:Provenance
.
dgn-np:NP387580.RA8GLOETG7mvZvhxqCH_E7wPgfJ0C9D91zcoTcm_6OCUk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP387580.RA8GLOETG7mvZvhxqCH_E7wPgfJ0C9D91zcoTcm_6OCUk130_assertion
{
miriam-gene:7515
a
ncit:C16612
.
lld:C0268529
a
ncit:C7057
.
dgn-gda:DGN93ef494ec289cdaeb0e3f9d93da9f55e
sio:SIO_000628
miriam-gene:7515
,
lld:C0268529
;
a
sio:SIO_001121
.
}
dgn-np:NP387580.RA8GLOETG7mvZvhxqCH_E7wPgfJ0C9D91zcoTcm_6OCUk130_provenance
{
dgn-np:NP387580.RA8GLOETG7mvZvhxqCH_E7wPgfJ0C9D91zcoTcm_6OCUk130_assertion
dcterms:description
"[Individuals with one or two XRCC1(R280H) variant alleles exhibited significantly higher TM values, and these differences were enhanced by alcohol consumption and aging, whereas smoking and poor HPI may cover up the differences.]. 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:18800344
;
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:NP387580.RA8GLOETG7mvZvhxqCH_E7wPgfJ0C9D91zcoTcm_6OCUk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:50+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" .
}