@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP777834.RABIwydcm-LWfQszQdodLEB-UuJdrZjQYIvQmd9kLxrVs
> .
@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:NP777834.RABIwydcm-LWfQszQdodLEB-UuJdrZjQYIvQmd9kLxrVs130_head
{
this:
np:hasAssertion
dgn-np:NP777834.RABIwydcm-LWfQszQdodLEB-UuJdrZjQYIvQmd9kLxrVs130_assertion
;
np:hasProvenance
dgn-np:NP777834.RABIwydcm-LWfQszQdodLEB-UuJdrZjQYIvQmd9kLxrVs130_provenance
;
np:hasPublicationInfo
dgn-np:NP777834.RABIwydcm-LWfQszQdodLEB-UuJdrZjQYIvQmd9kLxrVs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP777834.RABIwydcm-LWfQszQdodLEB-UuJdrZjQYIvQmd9kLxrVs130_assertion
a
np:Assertion
.
dgn-np:NP777834.RABIwydcm-LWfQszQdodLEB-UuJdrZjQYIvQmd9kLxrVs130_provenance
a
np:Provenance
.
dgn-np:NP777834.RABIwydcm-LWfQszQdodLEB-UuJdrZjQYIvQmd9kLxrVs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP777834.RABIwydcm-LWfQszQdodLEB-UuJdrZjQYIvQmd9kLxrVs130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0751676
a
ncit:C7057
.
dgn-gda:DGN5164ed5d9b6f54b7249361656aa7f4b2
sio:SIO_000628
miriam-gene:7157
,
lld:C0751676
;
a
sio:SIO_001121
.
}
dgn-np:NP777834.RABIwydcm-LWfQszQdodLEB-UuJdrZjQYIvQmd9kLxrVs130_provenance
{
dgn-np:NP777834.RABIwydcm-LWfQszQdodLEB-UuJdrZjQYIvQmd9kLxrVs130_assertion
dcterms:description
"[A patient with xeroderma pigmentosum group C was extensively examined for mutations in the p53 gene in normal skin exposed to varying degrees of sunlight and in excisional biopsies of basal cell cancer, squamous cell cancer, and squamous cell dysplasia.]. 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:9622088
;
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:NP777834.RABIwydcm-LWfQszQdodLEB-UuJdrZjQYIvQmd9kLxrVs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}