@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP937503.RA9GL0xQvQBIP_n8v9u-3UCeoo_HoqkgAbQsUFTdbFJAQ
> .
@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:NP937503.RA9GL0xQvQBIP_n8v9u-3UCeoo_HoqkgAbQsUFTdbFJAQ130_head
{
this:
np:hasAssertion
dgn-np:NP937503.RA9GL0xQvQBIP_n8v9u-3UCeoo_HoqkgAbQsUFTdbFJAQ130_assertion
;
np:hasProvenance
dgn-np:NP937503.RA9GL0xQvQBIP_n8v9u-3UCeoo_HoqkgAbQsUFTdbFJAQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP937503.RA9GL0xQvQBIP_n8v9u-3UCeoo_HoqkgAbQsUFTdbFJAQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP937503.RA9GL0xQvQBIP_n8v9u-3UCeoo_HoqkgAbQsUFTdbFJAQ130_assertion
a
np:Assertion
.
dgn-np:NP937503.RA9GL0xQvQBIP_n8v9u-3UCeoo_HoqkgAbQsUFTdbFJAQ130_provenance
a
np:Provenance
.
dgn-np:NP937503.RA9GL0xQvQBIP_n8v9u-3UCeoo_HoqkgAbQsUFTdbFJAQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP937503.RA9GL0xQvQBIP_n8v9u-3UCeoo_HoqkgAbQsUFTdbFJAQ130_assertion
{
miriam-gene:5727
a
ncit:C16612
.
lld:C0699893
a
ncit:C7057
.
dgn-gda:DGN231291b42b7f35eb5ea709c088d6ceb9
sio:SIO_000628
miriam-gene:5727
,
lld:C0699893
;
a
sio:SIO_001121
.
}
dgn-np:NP937503.RA9GL0xQvQBIP_n8v9u-3UCeoo_HoqkgAbQsUFTdbFJAQ130_provenance
{
dgn-np:NP937503.RA9GL0xQvQBIP_n8v9u-3UCeoo_HoqkgAbQsUFTdbFJAQ130_assertion
dcterms:description
"[Although our results do not exclude the presence of clonal alterations of the PTCH gene in skin cancers or mutations in other exons that were not screened, the present data do not support the presence of frequent mutations reported for non-melanoma skin cancer of other populations.]. 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:12700822
;
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:NP937503.RA9GL0xQvQBIP_n8v9u-3UCeoo_HoqkgAbQsUFTdbFJAQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:34+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" .
}