@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP552033.RAXusnd98uchzPScwx5U-daMty4n0DWw6ZtYt246bjUOc
> .
@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:NP552033.RAXusnd98uchzPScwx5U-daMty4n0DWw6ZtYt246bjUOc130_head
{
this:
np:hasAssertion
dgn-np:NP552033.RAXusnd98uchzPScwx5U-daMty4n0DWw6ZtYt246bjUOc130_assertion
;
np:hasProvenance
dgn-np:NP552033.RAXusnd98uchzPScwx5U-daMty4n0DWw6ZtYt246bjUOc130_provenance
;
np:hasPublicationInfo
dgn-np:NP552033.RAXusnd98uchzPScwx5U-daMty4n0DWw6ZtYt246bjUOc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP552033.RAXusnd98uchzPScwx5U-daMty4n0DWw6ZtYt246bjUOc130_assertion
a
np:Assertion
.
dgn-np:NP552033.RAXusnd98uchzPScwx5U-daMty4n0DWw6ZtYt246bjUOc130_provenance
a
np:Provenance
.
dgn-np:NP552033.RAXusnd98uchzPScwx5U-daMty4n0DWw6ZtYt246bjUOc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP552033.RAXusnd98uchzPScwx5U-daMty4n0DWw6ZtYt246bjUOc130_assertion
{
miriam-gene:5727
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN02ebf4254a216c04ddf7dd7d9bfe1b19
sio:SIO_000628
miriam-gene:5727
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP552033.RAXusnd98uchzPScwx5U-daMty4n0DWw6ZtYt246bjUOc130_provenance
{
dgn-np:NP552033.RAXusnd98uchzPScwx5U-daMty4n0DWw6ZtYt246bjUOc130_assertion
dcterms:description
"[The involvement of two tumor suppressors p16 and Ptch in pathogenesis of cutaneous melanomas and basal cell carcinomas (BCCs) was studied through expression of Ptch and p16 and genetic alterations in 9p21 region (p16) and in 9q22.3 region (PTCH) of chromosome 9.]. 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:19287961
;
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:NP552033.RAXusnd98uchzPScwx5U-daMty4n0DWw6ZtYt246bjUOc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:33+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" .
}