@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE
> .
@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:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_head
{
this:
np:hasAssertion
dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_assertion
;
np:hasProvenance
dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_provenance
;
np:hasPublicationInfo
dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_assertion
a
np:Assertion
.
dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_provenance
a
np:Provenance
.
dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_assertion
{
miriam-gene:5727
a
ncit:C16612
.
lld:C0002448
a
ncit:C7057
.
dgn-gda:DGNad593c44b9adc79032c5afe9afc186dc
sio:SIO_000628
miriam-gene:5727
,
lld:C0002448
;
a
sio:SIO_001121
.
}
dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_provenance
{
dgn-np:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_assertion
dcterms:description
"[Only five other cases of association between ameloblastoma and NBCCS have been reported so far, suggesting that PTCH1 missense mutation might take part in the pathogenesis of keratocystic odontogenic tumors (KCOTs) as well as ameloblastomas.]. 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:22559979
;
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:NP789926.RAd0bc-4QYVIXEzHY7FS357QbYpcFScluPMeohk22mijE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:05+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" .
}