@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP256348.RABiIjgpfpJWwqV8ZaRFhodMJIuNjv-6YHfSjRnVflYgM
> .
@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:NP256348.RABiIjgpfpJWwqV8ZaRFhodMJIuNjv-6YHfSjRnVflYgM130_head
{
this:
np:hasAssertion
dgn-np:NP256348.RABiIjgpfpJWwqV8ZaRFhodMJIuNjv-6YHfSjRnVflYgM130_assertion
;
np:hasProvenance
dgn-np:NP256348.RABiIjgpfpJWwqV8ZaRFhodMJIuNjv-6YHfSjRnVflYgM130_provenance
;
np:hasPublicationInfo
dgn-np:NP256348.RABiIjgpfpJWwqV8ZaRFhodMJIuNjv-6YHfSjRnVflYgM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP256348.RABiIjgpfpJWwqV8ZaRFhodMJIuNjv-6YHfSjRnVflYgM130_assertion
a
np:Assertion
.
dgn-np:NP256348.RABiIjgpfpJWwqV8ZaRFhodMJIuNjv-6YHfSjRnVflYgM130_provenance
a
np:Provenance
.
dgn-np:NP256348.RABiIjgpfpJWwqV8ZaRFhodMJIuNjv-6YHfSjRnVflYgM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP256348.RABiIjgpfpJWwqV8ZaRFhodMJIuNjv-6YHfSjRnVflYgM130_assertion
{
miriam-gene:2735
a
ncit:C16612
.
lld:C0699893
a
ncit:C7057
.
dgn-gda:DGNb65ad0cb8936cd5e2f0b8ef63f8fae2e
sio:SIO_000628
miriam-gene:2735
,
lld:C0699893
;
a
sio:SIO_001121
.
}
dgn-np:NP256348.RABiIjgpfpJWwqV8ZaRFhodMJIuNjv-6YHfSjRnVflYgM130_provenance
{
dgn-np:NP256348.RABiIjgpfpJWwqV8ZaRFhodMJIuNjv-6YHfSjRnVflYgM130_assertion
dcterms:description
"[Constitutive activation of hedgehog signaling, often caused by PTCH1 inactivation and leading to inappropriate activation of GLI target genes, is crucial for the development of several human tumors including basal cell carcinoma of the skin and medulloblastoma.]. 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:15521068
;
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:NP256348.RABiIjgpfpJWwqV8ZaRFhodMJIuNjv-6YHfSjRnVflYgM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:23+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" .
}