@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP859788.RAOHjhq4Yy4oit6l48JvRUn7Hq6NrxZOEg0F76ViiVBCY
> .
@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:NP859788.RAOHjhq4Yy4oit6l48JvRUn7Hq6NrxZOEg0F76ViiVBCY130_head
{
this:
np:hasAssertion
dgn-np:NP859788.RAOHjhq4Yy4oit6l48JvRUn7Hq6NrxZOEg0F76ViiVBCY130_assertion
;
np:hasProvenance
dgn-np:NP859788.RAOHjhq4Yy4oit6l48JvRUn7Hq6NrxZOEg0F76ViiVBCY130_provenance
;
np:hasPublicationInfo
dgn-np:NP859788.RAOHjhq4Yy4oit6l48JvRUn7Hq6NrxZOEg0F76ViiVBCY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP859788.RAOHjhq4Yy4oit6l48JvRUn7Hq6NrxZOEg0F76ViiVBCY130_assertion
a
np:Assertion
.
dgn-np:NP859788.RAOHjhq4Yy4oit6l48JvRUn7Hq6NrxZOEg0F76ViiVBCY130_provenance
a
np:Provenance
.
dgn-np:NP859788.RAOHjhq4Yy4oit6l48JvRUn7Hq6NrxZOEg0F76ViiVBCY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP859788.RAOHjhq4Yy4oit6l48JvRUn7Hq6NrxZOEg0F76ViiVBCY130_assertion
{
miriam-gene:6469
a
ncit:C16612
.
lld:C0567439
a
ncit:C7057
.
dgn-gda:DGN26715d9f27adad362cb08867124f7074
sio:SIO_000628
miriam-gene:6469
,
lld:C0567439
;
a
sio:SIO_001121
.
}
dgn-np:NP859788.RAOHjhq4Yy4oit6l48JvRUn7Hq6NrxZOEg0F76ViiVBCY130_provenance
{
dgn-np:NP859788.RAOHjhq4Yy4oit6l48JvRUn7Hq6NrxZOEg0F76ViiVBCY130_assertion
dcterms:description
"[Mutations in the receptor of SHH, the patched gene, have been characterized in sporadic BCCs as well as those from patients with the rare genetic syndromes nevoid BCC and xeroderma pigmentosum (XP).]. 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:12499255
;
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:NP859788.RAOHjhq4Yy4oit6l48JvRUn7Hq6NrxZOEg0F76ViiVBCY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:45+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" .
}