@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP272177.RAKb7Ox1rLiIMi2zQFkbeg2uMAH5eAYfbHHJy4p398rYI
> .
@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:NP272177.RAKb7Ox1rLiIMi2zQFkbeg2uMAH5eAYfbHHJy4p398rYI130_head
{
this:
np:hasAssertion
dgn-np:NP272177.RAKb7Ox1rLiIMi2zQFkbeg2uMAH5eAYfbHHJy4p398rYI130_assertion
;
np:hasProvenance
dgn-np:NP272177.RAKb7Ox1rLiIMi2zQFkbeg2uMAH5eAYfbHHJy4p398rYI130_provenance
;
np:hasPublicationInfo
dgn-np:NP272177.RAKb7Ox1rLiIMi2zQFkbeg2uMAH5eAYfbHHJy4p398rYI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP272177.RAKb7Ox1rLiIMi2zQFkbeg2uMAH5eAYfbHHJy4p398rYI130_assertion
a
np:Assertion
.
dgn-np:NP272177.RAKb7Ox1rLiIMi2zQFkbeg2uMAH5eAYfbHHJy4p398rYI130_provenance
a
np:Provenance
.
dgn-np:NP272177.RAKb7Ox1rLiIMi2zQFkbeg2uMAH5eAYfbHHJy4p398rYI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP272177.RAKb7Ox1rLiIMi2zQFkbeg2uMAH5eAYfbHHJy4p398rYI130_assertion
{
miriam-gene:2952
a
ncit:C16612
.
lld:C0699791
a
ncit:C7057
.
dgn-gda:DGNb948b60074568c361e32ae468c848583
sio:SIO_000628
miriam-gene:2952
,
lld:C0699791
;
a
sio:SIO_001121
.
}
dgn-np:NP272177.RAKb7Ox1rLiIMi2zQFkbeg2uMAH5eAYfbHHJy4p398rYI130_provenance
{
dgn-np:NP272177.RAKb7Ox1rLiIMi2zQFkbeg2uMAH5eAYfbHHJy4p398rYI130_assertion
dcterms:description
"[XRCC1 codon 194 Trp carrier status is correlated with more aggressive biological behavior of GC, such as venous invasion, and the GSTT1 null genotype is associated with better survival in GC patients.]. 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:21378360
;
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:NP272177.RAKb7Ox1rLiIMi2zQFkbeg2uMAH5eAYfbHHJy4p398rYI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:33+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" .
}