@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP821425.RA7zr0CS42vesxQwsDsq7gamhbB2W4s6VnlbiF8WPrFWI
> .
@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:NP821425.RA7zr0CS42vesxQwsDsq7gamhbB2W4s6VnlbiF8WPrFWI130_head
{
this:
np:hasAssertion
dgn-np:NP821425.RA7zr0CS42vesxQwsDsq7gamhbB2W4s6VnlbiF8WPrFWI130_assertion
;
np:hasProvenance
dgn-np:NP821425.RA7zr0CS42vesxQwsDsq7gamhbB2W4s6VnlbiF8WPrFWI130_provenance
;
np:hasPublicationInfo
dgn-np:NP821425.RA7zr0CS42vesxQwsDsq7gamhbB2W4s6VnlbiF8WPrFWI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP821425.RA7zr0CS42vesxQwsDsq7gamhbB2W4s6VnlbiF8WPrFWI130_assertion
a
np:Assertion
.
dgn-np:NP821425.RA7zr0CS42vesxQwsDsq7gamhbB2W4s6VnlbiF8WPrFWI130_provenance
a
np:Provenance
.
dgn-np:NP821425.RA7zr0CS42vesxQwsDsq7gamhbB2W4s6VnlbiF8WPrFWI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP821425.RA7zr0CS42vesxQwsDsq7gamhbB2W4s6VnlbiF8WPrFWI130_assertion
{
miriam-gene:64754
a
ncit:C16612
.
lld:C0006142
a
ncit:C7057
.
dgn-gda:DGNa1bafa2a101c1387d1b8bdc2a2ffbdf3
sio:SIO_000628
miriam-gene:64754
,
lld:C0006142
;
a
sio:SIO_001121
.
}
dgn-np:NP821425.RA7zr0CS42vesxQwsDsq7gamhbB2W4s6VnlbiF8WPrFWI130_provenance
{
dgn-np:NP821425.RA7zr0CS42vesxQwsDsq7gamhbB2W4s6VnlbiF8WPrFWI130_assertion
dcterms:description
"[A variable number of tandem repeats (VNTR) polymorphism in regulatory region of SMYD3 coding for histone methyltransferase has been shown to be associated with colorectal cancer, hepatocellular carcinoma (HCC), and breast cancer in Japanese population.]. 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:17431393
;
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:NP821425.RA7zr0CS42vesxQwsDsq7gamhbB2W4s6VnlbiF8WPrFWI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:23+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" .
}