@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP399224.RAyZLlBxJ6s2pPs_END9TUPV4lZOxXQuII0VlXjxoRFD0
> .
@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:NP399224.RAyZLlBxJ6s2pPs_END9TUPV4lZOxXQuII0VlXjxoRFD0130_head
{
this:
np:hasAssertion
dgn-np:NP399224.RAyZLlBxJ6s2pPs_END9TUPV4lZOxXQuII0VlXjxoRFD0130_assertion
;
np:hasProvenance
dgn-np:NP399224.RAyZLlBxJ6s2pPs_END9TUPV4lZOxXQuII0VlXjxoRFD0130_provenance
;
np:hasPublicationInfo
dgn-np:NP399224.RAyZLlBxJ6s2pPs_END9TUPV4lZOxXQuII0VlXjxoRFD0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP399224.RAyZLlBxJ6s2pPs_END9TUPV4lZOxXQuII0VlXjxoRFD0130_assertion
a
np:Assertion
.
dgn-np:NP399224.RAyZLlBxJ6s2pPs_END9TUPV4lZOxXQuII0VlXjxoRFD0130_provenance
a
np:Provenance
.
dgn-np:NP399224.RAyZLlBxJ6s2pPs_END9TUPV4lZOxXQuII0VlXjxoRFD0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP399224.RAyZLlBxJ6s2pPs_END9TUPV4lZOxXQuII0VlXjxoRFD0130_assertion
{
miriam-gene:4193
a
ncit:C16612
.
lld:C0005684
a
ncit:C7057
.
dgn-gda:DGN90ce50860574b8719efe32a265c9aeb4
sio:SIO_000628
miriam-gene:4193
,
lld:C0005684
;
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sio:SIO_001121
.
}
dgn-np:NP399224.RAyZLlBxJ6s2pPs_END9TUPV4lZOxXQuII0VlXjxoRFD0130_provenance
{
dgn-np:NP399224.RAyZLlBxJ6s2pPs_END9TUPV4lZOxXQuII0VlXjxoRFD0130_assertion
dcterms:description
"[We found that the C1797G polymorphism in the MDM2 promoter region is an important SNP because its homozygous variant genotype, but none of the haplotypes, was associated with risk of bladder cancer.]. 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:18519798
;
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:NP399224.RAyZLlBxJ6s2pPs_END9TUPV4lZOxXQuII0VlXjxoRFD0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:58+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
<
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> , <
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" .
}