@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP497954.RA8KuOe8vGcssEghkxE62IQXfXj8ygufJei6thu3Q_zLM
> .
@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:NP497954.RA8KuOe8vGcssEghkxE62IQXfXj8ygufJei6thu3Q_zLM130_head
{
this:
np:hasAssertion
dgn-np:NP497954.RA8KuOe8vGcssEghkxE62IQXfXj8ygufJei6thu3Q_zLM130_assertion
;
np:hasProvenance
dgn-np:NP497954.RA8KuOe8vGcssEghkxE62IQXfXj8ygufJei6thu3Q_zLM130_provenance
;
np:hasPublicationInfo
dgn-np:NP497954.RA8KuOe8vGcssEghkxE62IQXfXj8ygufJei6thu3Q_zLM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP497954.RA8KuOe8vGcssEghkxE62IQXfXj8ygufJei6thu3Q_zLM130_assertion
a
np:Assertion
.
dgn-np:NP497954.RA8KuOe8vGcssEghkxE62IQXfXj8ygufJei6thu3Q_zLM130_provenance
a
np:Provenance
.
dgn-np:NP497954.RA8KuOe8vGcssEghkxE62IQXfXj8ygufJei6thu3Q_zLM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP497954.RA8KuOe8vGcssEghkxE62IQXfXj8ygufJei6thu3Q_zLM130_assertion
{
miriam-gene:1499
a
ncit:C16612
.
lld:C0002448
a
ncit:C7057
.
dgn-gda:DGN37b6befdac28f62b44aeb8bd7d1c7ce0
sio:SIO_000628
miriam-gene:1499
,
lld:C0002448
;
a
sio:SIO_001121
.
}
dgn-np:NP497954.RA8KuOe8vGcssEghkxE62IQXfXj8ygufJei6thu3Q_zLM130_provenance
{
dgn-np:NP497954.RA8KuOe8vGcssEghkxE62IQXfXj8ygufJei6thu3Q_zLM130_assertion
dcterms:description
"[Six ameloblastomas (five follicular ameloblastomas and one plexiform ameloblastoma) and three malignant odontogenic tumors (one metastasizing ameloblastoma, one ameloblastic carcinoma, and one primary intraosseous odontogenic carcinoma) were investigated for CTNNB1 expression and CTNNB1 mutation.]. 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:17096730
;
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:NP497954.RA8KuOe8vGcssEghkxE62IQXfXj8ygufJei6thu3Q_zLM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:57+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" .
}