@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP341008.RA7l35z05tF3fgmx15XTMVK5pOhYBHdMOZnMLyn5VeBzY
> .
@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:NP341008.RA7l35z05tF3fgmx15XTMVK5pOhYBHdMOZnMLyn5VeBzY130_head
{
this:
np:hasAssertion
dgn-np:NP341008.RA7l35z05tF3fgmx15XTMVK5pOhYBHdMOZnMLyn5VeBzY130_assertion
;
np:hasProvenance
dgn-np:NP341008.RA7l35z05tF3fgmx15XTMVK5pOhYBHdMOZnMLyn5VeBzY130_provenance
;
np:hasPublicationInfo
dgn-np:NP341008.RA7l35z05tF3fgmx15XTMVK5pOhYBHdMOZnMLyn5VeBzY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP341008.RA7l35z05tF3fgmx15XTMVK5pOhYBHdMOZnMLyn5VeBzY130_assertion
a
np:Assertion
.
dgn-np:NP341008.RA7l35z05tF3fgmx15XTMVK5pOhYBHdMOZnMLyn5VeBzY130_provenance
a
np:Provenance
.
dgn-np:NP341008.RA7l35z05tF3fgmx15XTMVK5pOhYBHdMOZnMLyn5VeBzY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP341008.RA7l35z05tF3fgmx15XTMVK5pOhYBHdMOZnMLyn5VeBzY130_assertion
{
miriam-gene:124872
a
ncit:C16612
.
lld:C0699791
a
ncit:C7057
.
dgn-gda:DGN913a5651c3d6e720363b9c514e468504
sio:SIO_000628
miriam-gene:124872
,
lld:C0699791
;
a
sio:SIO_001121
.
}
dgn-np:NP341008.RA7l35z05tF3fgmx15XTMVK5pOhYBHdMOZnMLyn5VeBzY130_provenance
{
dgn-np:NP341008.RA7l35z05tF3fgmx15XTMVK5pOhYBHdMOZnMLyn5VeBzY130_assertion
dcterms:description
"[The promoter region of the human B4GALNT2 gene was heavily hypermethylated in many of the GI cancer cell lines examined as well as in gastric cancer tissues (39 out of 78 cases).]. 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:18485915
;
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:NP341008.RA7l35z05tF3fgmx15XTMVK5pOhYBHdMOZnMLyn5VeBzY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:20+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" .
}