@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP620968.RAgQZKYUOhR8drH--hrwzjWf9iBiGezbcPMJOk9qYDfBo
> .
@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:NP620968.RAgQZKYUOhR8drH--hrwzjWf9iBiGezbcPMJOk9qYDfBo130_head
{
this:
np:hasAssertion
dgn-np:NP620968.RAgQZKYUOhR8drH--hrwzjWf9iBiGezbcPMJOk9qYDfBo130_assertion
;
np:hasProvenance
dgn-np:NP620968.RAgQZKYUOhR8drH--hrwzjWf9iBiGezbcPMJOk9qYDfBo130_provenance
;
np:hasPublicationInfo
dgn-np:NP620968.RAgQZKYUOhR8drH--hrwzjWf9iBiGezbcPMJOk9qYDfBo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP620968.RAgQZKYUOhR8drH--hrwzjWf9iBiGezbcPMJOk9qYDfBo130_assertion
a
np:Assertion
.
dgn-np:NP620968.RAgQZKYUOhR8drH--hrwzjWf9iBiGezbcPMJOk9qYDfBo130_provenance
a
np:Provenance
.
dgn-np:NP620968.RAgQZKYUOhR8drH--hrwzjWf9iBiGezbcPMJOk9qYDfBo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP620968.RAgQZKYUOhR8drH--hrwzjWf9iBiGezbcPMJOk9qYDfBo130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0279680
a
ncit:C7057
.
dgn-gda:DGNd881c509f68b266155b06cdd6d0b6aa4
sio:SIO_000628
miriam-gene:4524
,
lld:C0279680
;
a
sio:SIO_001121
.
}
dgn-np:NP620968.RAgQZKYUOhR8drH--hrwzjWf9iBiGezbcPMJOk9qYDfBo130_provenance
{
dgn-np:NP620968.RAgQZKYUOhR8drH--hrwzjWf9iBiGezbcPMJOk9qYDfBo130_assertion
dcterms:description
"[Because hypomethylation is particularly prevalent in transitional cell carcinoma of the urinary bladder (TCC), the genotype distributions for the two each most prevalent MTHFR, MS, and CBS alleles were compared between 165 TCC patients and 150 population controls.]. 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:11406421
;
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:NP620968.RAgQZKYUOhR8drH--hrwzjWf9iBiGezbcPMJOk9qYDfBo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:15+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" .
}