@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP665324.RAsYPKtL34V6W03FdVYK-tC9xUDrl_qYLURa3vVxitbBk
> .
@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:NP665324.RAsYPKtL34V6W03FdVYK-tC9xUDrl_qYLURa3vVxitbBk130_head
{
this:
np:hasAssertion
dgn-np:NP665324.RAsYPKtL34V6W03FdVYK-tC9xUDrl_qYLURa3vVxitbBk130_assertion
;
np:hasProvenance
dgn-np:NP665324.RAsYPKtL34V6W03FdVYK-tC9xUDrl_qYLURa3vVxitbBk130_provenance
;
np:hasPublicationInfo
dgn-np:NP665324.RAsYPKtL34V6W03FdVYK-tC9xUDrl_qYLURa3vVxitbBk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP665324.RAsYPKtL34V6W03FdVYK-tC9xUDrl_qYLURa3vVxitbBk130_assertion
a
np:Assertion
.
dgn-np:NP665324.RAsYPKtL34V6W03FdVYK-tC9xUDrl_qYLURa3vVxitbBk130_provenance
a
np:Provenance
.
dgn-np:NP665324.RAsYPKtL34V6W03FdVYK-tC9xUDrl_qYLURa3vVxitbBk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP665324.RAsYPKtL34V6W03FdVYK-tC9xUDrl_qYLURa3vVxitbBk130_assertion
{
miriam-gene:796
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGN26dee270f25563100a6c75e2b5056445
sio:SIO_000628
miriam-gene:796
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP665324.RAsYPKtL34V6W03FdVYK-tC9xUDrl_qYLURa3vVxitbBk130_provenance
{
dgn-np:NP665324.RAsYPKtL34V6W03FdVYK-tC9xUDrl_qYLURa3vVxitbBk130_assertion
dcterms:description
"[The increased methylation of the CT gene may then provide an important molecular marker for biologic events in human cell transformation or tumor progression and may prove clinically useful in monitoring patients with lymphoid and acute myelogenous neoplasms.]. 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:3607279
;
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:NP665324.RAsYPKtL34V6W03FdVYK-tC9xUDrl_qYLURa3vVxitbBk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:42+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" .
}