@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP861767.RAU1xSVdr9RPgSUN8fTiWhTzZX_2BmiWZKtyc8L-8tJtw
> .
@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:NP861767.RAU1xSVdr9RPgSUN8fTiWhTzZX_2BmiWZKtyc8L-8tJtw130_head
{
this:
np:hasAssertion
dgn-np:NP861767.RAU1xSVdr9RPgSUN8fTiWhTzZX_2BmiWZKtyc8L-8tJtw130_assertion
;
np:hasProvenance
dgn-np:NP861767.RAU1xSVdr9RPgSUN8fTiWhTzZX_2BmiWZKtyc8L-8tJtw130_provenance
;
np:hasPublicationInfo
dgn-np:NP861767.RAU1xSVdr9RPgSUN8fTiWhTzZX_2BmiWZKtyc8L-8tJtw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP861767.RAU1xSVdr9RPgSUN8fTiWhTzZX_2BmiWZKtyc8L-8tJtw130_assertion
a
np:Assertion
.
dgn-np:NP861767.RAU1xSVdr9RPgSUN8fTiWhTzZX_2BmiWZKtyc8L-8tJtw130_provenance
a
np:Provenance
.
dgn-np:NP861767.RAU1xSVdr9RPgSUN8fTiWhTzZX_2BmiWZKtyc8L-8tJtw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP861767.RAU1xSVdr9RPgSUN8fTiWhTzZX_2BmiWZKtyc8L-8tJtw130_assertion
{
miriam-gene:6469
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN11febd6ffa04e792c7bb876671108a9f
sio:SIO_000628
miriam-gene:6469
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP861767.RAU1xSVdr9RPgSUN8fTiWhTzZX_2BmiWZKtyc8L-8tJtw130_provenance
{
dgn-np:NP861767.RAU1xSVdr9RPgSUN8fTiWhTzZX_2BmiWZKtyc8L-8tJtw130_assertion
dcterms:description
"[These data indicate that expression of SHH in human skin recapitulates features of human BCC in vivo, suggest that activation of this conserved signaling pathway contributes to the development of epithelial neoplasia and describe a new transgenic human tissue model of neoplasia.]. 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:9212109
;
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:NP861767.RAU1xSVdr9RPgSUN8fTiWhTzZX_2BmiWZKtyc8L-8tJtw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:47+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" .
}