@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA
> .
@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:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_head
{
this:
np:hasAssertion
dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_assertion
;
np:hasProvenance
dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_provenance
;
np:hasPublicationInfo
dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_assertion
a
np:Assertion
.
dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_provenance
a
np:Provenance
.
dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_assertion
{
miriam-gene:64754
a
ncit:C16612
.
lld:C0596263
a
ncit:C7057
.
dgn-gda:DGN8c5bd69ff399c67872af2b6fa760ecba
sio:SIO_000628
miriam-gene:64754
,
lld:C0596263
;
a
sio:SIO_001121
.
}
dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_provenance
{
dgn-np:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_assertion
dcterms:description
"[A variable number of tandem repeats (VNTR) polymorphism in the promoter region of SMYD3, a recently characterized histone lysine methyltransferase gene that is implicated in cell proliferation and carcinogenesis, has been shown to be functional, but its association with cancer risk has not been well established because of apparently discrepant results in different populations.]. 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:18294291
;
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:NP704363.RAdqgQMPu7iF-TZlaTet2NB0YOAB2RwfE24QhNrxcb9CA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:08+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" .
}