@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_assertion
;
np:hasProvenance
dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_provenance
;
np:hasPublicationInfo
dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_assertion
a
np:Assertion
.
dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_provenance
a
np:Provenance
.
dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_assertion
{
miriam-gene:4360
a
ncit:C16612
.
lld:C0877373
a
ncit:C7057
.
dgn-gda:DGN92be3d6e6b2c9df34b3a812ec871414d
sio:SIO_000628
miriam-gene:4360
,
lld:C0877373
;
a
sio:SIO_001121
.
}
dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_provenance
{
dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_assertion
dcterms:description
"[One of the main reasons why most patients with advanced cancer are not curable with the therapies available is the broad heterogeneity of cancer cells, inherently related to their genomic instability that reflects defects of cell cycle checkpoints and DNA mismatch repair (MMR).]. 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:20840074
;
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 .
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dgn-np:NP917313.RAKJO2agW53oleB2h0IDOq_fbibA1Y_ARTP3B7PhEgdKg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:23+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
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pav:authoredBy
<
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> , <
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
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