@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP524689.RAxW8W21Zar5EKuzGzFSrMIFYsCCKLKzX3Lj2KvuuKSrc
> .
@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:NP524689.RAxW8W21Zar5EKuzGzFSrMIFYsCCKLKzX3Lj2KvuuKSrc130_head
{
this:
np:hasAssertion
dgn-np:NP524689.RAxW8W21Zar5EKuzGzFSrMIFYsCCKLKzX3Lj2KvuuKSrc130_assertion
;
np:hasProvenance
dgn-np:NP524689.RAxW8W21Zar5EKuzGzFSrMIFYsCCKLKzX3Lj2KvuuKSrc130_provenance
;
np:hasPublicationInfo
dgn-np:NP524689.RAxW8W21Zar5EKuzGzFSrMIFYsCCKLKzX3Lj2KvuuKSrc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP524689.RAxW8W21Zar5EKuzGzFSrMIFYsCCKLKzX3Lj2KvuuKSrc130_assertion
a
np:Assertion
.
dgn-np:NP524689.RAxW8W21Zar5EKuzGzFSrMIFYsCCKLKzX3Lj2KvuuKSrc130_provenance
a
np:Provenance
.
dgn-np:NP524689.RAxW8W21Zar5EKuzGzFSrMIFYsCCKLKzX3Lj2KvuuKSrc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP524689.RAxW8W21Zar5EKuzGzFSrMIFYsCCKLKzX3Lj2KvuuKSrc130_assertion
{
miriam-gene:7517
a
ncit:C16612
.
lld:C0009402
a
ncit:C7057
.
dgn-gda:DGNeeae810b53689bb7fad097354dbe3a18
sio:SIO_000628
miriam-gene:7517
,
lld:C0009402
;
a
sio:SIO_001121
.
}
dgn-np:NP524689.RAxW8W21Zar5EKuzGzFSrMIFYsCCKLKzX3Lj2KvuuKSrc130_provenance
{
dgn-np:NP524689.RAxW8W21Zar5EKuzGzFSrMIFYsCCKLKzX3Lj2KvuuKSrc130_assertion
dcterms:description
"[These results also suggest that XRCC3 T241M polymorphism and FH of cancer may be risk factors for CRC, and the XRCC3 241Met allele may be an effective biomarker for genetic susceptibility to CRC.]. 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:16271954
;
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:NP524689.RAxW8W21Zar5EKuzGzFSrMIFYsCCKLKzX3Lj2KvuuKSrc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:14+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" .
}