@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k
> .
@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:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_head
{
this:
np:hasAssertion
dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_assertion
;
np:hasProvenance
dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_provenance
;
np:hasPublicationInfo
dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_assertion
a
np:Assertion
.
dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_provenance
a
np:Provenance
.
dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_assertion
{
miriam-gene:7515
a
ncit:C16612
.
lld:C1527249
a
ncit:C7057
.
dgn-gda:DGN5836c85b780907df47ebb67139c1a9ce
sio:SIO_000628
miriam-gene:7515
,
lld:C1527249
;
a
sio:SIO_001121
.
}
dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_provenance
{
dgn-np:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_assertion
dcterms:description
"[Our meta-analysis provides an evidence for the association between XRCC1 Arg399Gln polymorphism and colorectal cancer risk in Chinese population, and XRCC1 Arg399Gln variant genotypes contribute to increased risk of colorectal cancer in Chinese.]. 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:23712778
;
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:NP177231.RAp6bfzP9C0VDWMbf5GQt1eFRktOHauUpGxRJlxGpa15k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:36+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" .
}