@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ
> .
@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:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_head
{
this:
np:hasAssertion
dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_assertion
;
np:hasProvenance
dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_assertion
a
np:Assertion
.
dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_provenance
a
np:Provenance
.
dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_assertion
{
miriam-gene:6469
a
ncit:C16612
.
lld:C0004779
a
ncit:C7057
.
dgn-gda:DGN8f0ca64cff2cd42d255fc0aa0d845ee9
sio:SIO_000628
miriam-gene:6469
,
lld:C0004779
;
a
sio:SIO_001121
.
}
dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_provenance
{
dgn-np:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_assertion
dcterms:description
"[Loss-of-function mutations in Patched (Ptch1) are implicated in constitutive activation of the Sonic hedgehog pathway in human basal cell carcinomas (BCCs), and inherited Ptch1 mutations underlie basal cell nevus syndrome in which a typical feature is multiple BCC occurring with greater incidence in portals of radiotherapy.]. 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:14871823
;
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:NP278571.RADUoF7tIl2NpzZs2ymY_OC5-sajeurYLtIjtVE2Qv3AQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:37+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" .
}