@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP901792.RA5-OnyoJ_5xCXswyAYaezBjq1lb0r74VtsTc9i0JVLMQ
> .
@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:NP901792.RA5-OnyoJ_5xCXswyAYaezBjq1lb0r74VtsTc9i0JVLMQ130_head
{
this:
np:hasAssertion
dgn-np:NP901792.RA5-OnyoJ_5xCXswyAYaezBjq1lb0r74VtsTc9i0JVLMQ130_assertion
;
np:hasProvenance
dgn-np:NP901792.RA5-OnyoJ_5xCXswyAYaezBjq1lb0r74VtsTc9i0JVLMQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP901792.RA5-OnyoJ_5xCXswyAYaezBjq1lb0r74VtsTc9i0JVLMQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP901792.RA5-OnyoJ_5xCXswyAYaezBjq1lb0r74VtsTc9i0JVLMQ130_assertion
a
np:Assertion
.
dgn-np:NP901792.RA5-OnyoJ_5xCXswyAYaezBjq1lb0r74VtsTc9i0JVLMQ130_provenance
a
np:Provenance
.
dgn-np:NP901792.RA5-OnyoJ_5xCXswyAYaezBjq1lb0r74VtsTc9i0JVLMQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP901792.RA5-OnyoJ_5xCXswyAYaezBjq1lb0r74VtsTc9i0JVLMQ130_assertion
{
miriam-gene:1111
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN398aacb883f8e8f335528b41abc220a8
sio:SIO_000628
miriam-gene:1111
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP901792.RA5-OnyoJ_5xCXswyAYaezBjq1lb0r74VtsTc9i0JVLMQ130_provenance
{
dgn-np:NP901792.RA5-OnyoJ_5xCXswyAYaezBjq1lb0r74VtsTc9i0JVLMQ130_assertion
dcterms:description
"[It also suggests that markers of DNA damage may be useful in identifying the melanomas and potentially other tumour types that are more likely to be sensitive to Chk1 inhibitors as single agents.]. 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:22391562
;
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:NP901792.RA5-OnyoJ_5xCXswyAYaezBjq1lb0r74VtsTc9i0JVLMQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:14+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" .
}