@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM
> .
@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:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_head
{
this:
np:hasAssertion
dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_assertion
;
np:hasProvenance
dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_provenance
;
np:hasPublicationInfo
dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_assertion
a
np:Assertion
.
dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_provenance
a
np:Provenance
.
dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_assertion
{
miriam-gene:5727
a
ncit:C16612
.
lld:C1333190
a
ncit:C7057
.
dgn-gda:DGNd54a27261b6b7eb866ad9e1e054bb1a3
sio:SIO_000628
miriam-gene:5727
,
lld:C1333190
;
a
sio:SIO_001121
.
}
dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_provenance
{
dgn-np:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_assertion
dcterms:description
"[Recent advances in genetic and molecular research, i.e., PTCH1 mutations and involvement of the Hedgehog signaling pathway, have led to increased knowledge of OKC pathogenesis which hints at potential new treatment options, although the question of whether the OKC is a cyst or a cystic neoplasm is yet to be answered with certainty.]. 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:21270459
;
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:NP696180.RATg7nWsAfsxecLS--ViF_4nvhWITbw3dqRUB8njE8tfM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:03+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" .
}