@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP228888.RAGejty9VFCPxh7yjkWqYIVurgsZ5bZy4CDCYoPQAQP0o
> .
@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:NP228888.RAGejty9VFCPxh7yjkWqYIVurgsZ5bZy4CDCYoPQAQP0o130_head
{
this:
np:hasAssertion
dgn-np:NP228888.RAGejty9VFCPxh7yjkWqYIVurgsZ5bZy4CDCYoPQAQP0o130_assertion
;
np:hasProvenance
dgn-np:NP228888.RAGejty9VFCPxh7yjkWqYIVurgsZ5bZy4CDCYoPQAQP0o130_provenance
;
np:hasPublicationInfo
dgn-np:NP228888.RAGejty9VFCPxh7yjkWqYIVurgsZ5bZy4CDCYoPQAQP0o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP228888.RAGejty9VFCPxh7yjkWqYIVurgsZ5bZy4CDCYoPQAQP0o130_assertion
a
np:Assertion
.
dgn-np:NP228888.RAGejty9VFCPxh7yjkWqYIVurgsZ5bZy4CDCYoPQAQP0o130_provenance
a
np:Provenance
.
dgn-np:NP228888.RAGejty9VFCPxh7yjkWqYIVurgsZ5bZy4CDCYoPQAQP0o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP228888.RAGejty9VFCPxh7yjkWqYIVurgsZ5bZy4CDCYoPQAQP0o130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0442867
a
ncit:C7057
.
dgn-gda:DGNde2551c85faf458b8f830808017ad126
sio:SIO_000628
miriam-gene:1029
,
lld:C0442867
;
a
sio:SIO_001121
.
}
dgn-np:NP228888.RAGejty9VFCPxh7yjkWqYIVurgsZ5bZy4CDCYoPQAQP0o130_provenance
{
dgn-np:NP228888.RAGejty9VFCPxh7yjkWqYIVurgsZ5bZy4CDCYoPQAQP0o130_assertion
dcterms:description
"[Human urothelial cell carcinoma evolves via the accumulation of numerous genetic alterations, with loss of p53 and p16 function representing important stages in the development of superficial lesions and their progression to malignant disease.]. 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:15825166
;
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:NP228888.RAGejty9VFCPxh7yjkWqYIVurgsZ5bZy4CDCYoPQAQP0o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:08+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" .
}