@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP429875.RAu84EgTfFvJ0zRUFFJCRJIVuQwAmVcYps0Qvhh80TN_s
> .
@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:NP429875.RAu84EgTfFvJ0zRUFFJCRJIVuQwAmVcYps0Qvhh80TN_s130_head
{
this:
np:hasAssertion
dgn-np:NP429875.RAu84EgTfFvJ0zRUFFJCRJIVuQwAmVcYps0Qvhh80TN_s130_assertion
;
np:hasProvenance
dgn-np:NP429875.RAu84EgTfFvJ0zRUFFJCRJIVuQwAmVcYps0Qvhh80TN_s130_provenance
;
np:hasPublicationInfo
dgn-np:NP429875.RAu84EgTfFvJ0zRUFFJCRJIVuQwAmVcYps0Qvhh80TN_s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP429875.RAu84EgTfFvJ0zRUFFJCRJIVuQwAmVcYps0Qvhh80TN_s130_assertion
a
np:Assertion
.
dgn-np:NP429875.RAu84EgTfFvJ0zRUFFJCRJIVuQwAmVcYps0Qvhh80TN_s130_provenance
a
np:Provenance
.
dgn-np:NP429875.RAu84EgTfFvJ0zRUFFJCRJIVuQwAmVcYps0Qvhh80TN_s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP429875.RAu84EgTfFvJ0zRUFFJCRJIVuQwAmVcYps0Qvhh80TN_s130_assertion
{
miriam-gene:5727
a
ncit:C16612
.
lld:C0025149
a
ncit:C7057
.
dgn-gda:DGNfbf31868b384d2e9f7e50d67a25e69f4
sio:SIO_000628
miriam-gene:5727
,
lld:C0025149
;
a
sio:SIO_001121
.
}
dgn-np:NP429875.RAu84EgTfFvJ0zRUFFJCRJIVuQwAmVcYps0Qvhh80TN_s130_provenance
{
dgn-np:NP429875.RAu84EgTfFvJ0zRUFFJCRJIVuQwAmVcYps0Qvhh80TN_s130_assertion
dcterms:description
"[It now appears that constitutive activation of Hedgehog signalling, by inactivating mutations in PTCH1 or activating mutations in the coreceptor SMOH, is required and possibly sufficient for basal cell carcinoma development and also contributes to the formation of a variety of other tumour types, including medulloblastoma and rhabdomyosarcoma.]. 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:11130178
;
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:NP429875.RAu84EgTfFvJ0zRUFFJCRJIVuQwAmVcYps0Qvhh80TN_s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:14+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" .
}