@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP381072.RAaJFRvKSqhfj6pJm6bD3k1rjKsvGwX2rrCey8JsrApTE
> .
@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:NP381072.RAaJFRvKSqhfj6pJm6bD3k1rjKsvGwX2rrCey8JsrApTE130_head
{
this:
np:hasAssertion
dgn-np:NP381072.RAaJFRvKSqhfj6pJm6bD3k1rjKsvGwX2rrCey8JsrApTE130_assertion
;
np:hasProvenance
dgn-np:NP381072.RAaJFRvKSqhfj6pJm6bD3k1rjKsvGwX2rrCey8JsrApTE130_provenance
;
np:hasPublicationInfo
dgn-np:NP381072.RAaJFRvKSqhfj6pJm6bD3k1rjKsvGwX2rrCey8JsrApTE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP381072.RAaJFRvKSqhfj6pJm6bD3k1rjKsvGwX2rrCey8JsrApTE130_assertion
a
np:Assertion
.
dgn-np:NP381072.RAaJFRvKSqhfj6pJm6bD3k1rjKsvGwX2rrCey8JsrApTE130_provenance
a
np:Provenance
.
dgn-np:NP381072.RAaJFRvKSqhfj6pJm6bD3k1rjKsvGwX2rrCey8JsrApTE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP381072.RAaJFRvKSqhfj6pJm6bD3k1rjKsvGwX2rrCey8JsrApTE130_assertion
{
miriam-gene:6817
a
ncit:C16612
.
lld:C0005684
a
ncit:C7057
.
dgn-gda:DGN1d8f9912fea20825338ec3515a713941
sio:SIO_000628
miriam-gene:6817
,
lld:C0005684
;
a
sio:SIO_001121
.
}
dgn-np:NP381072.RAaJFRvKSqhfj6pJm6bD3k1rjKsvGwX2rrCey8JsrApTE130_provenance
{
dgn-np:NP381072.RAaJFRvKSqhfj6pJm6bD3k1rjKsvGwX2rrCey8JsrApTE130_assertion
dcterms:description
"[Because of its functional role and published data showing the influence of Arg213His polymorphism on the risk of some cancers, we hypothesized that the His(213) allele of the SULT1A1 gene may modify bladder cancer risk.]. 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:14643027
;
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:NP381072.RAaJFRvKSqhfj6pJm6bD3k1rjKsvGwX2rrCey8JsrApTE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:45+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" .
}