@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP11753.RAqhubQ14A-512VnJsQgQLEwShqdvvurQW6pQGgtYGysk
> .
@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:NP11753.RAqhubQ14A-512VnJsQgQLEwShqdvvurQW6pQGgtYGysk130_head
{
this:
np:hasAssertion
dgn-np:NP11753.RAqhubQ14A-512VnJsQgQLEwShqdvvurQW6pQGgtYGysk130_assertion
;
np:hasProvenance
dgn-np:NP11753.RAqhubQ14A-512VnJsQgQLEwShqdvvurQW6pQGgtYGysk130_provenance
;
np:hasPublicationInfo
dgn-np:NP11753.RAqhubQ14A-512VnJsQgQLEwShqdvvurQW6pQGgtYGysk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP11753.RAqhubQ14A-512VnJsQgQLEwShqdvvurQW6pQGgtYGysk130_assertion
a
np:Assertion
.
dgn-np:NP11753.RAqhubQ14A-512VnJsQgQLEwShqdvvurQW6pQGgtYGysk130_provenance
a
np:Provenance
.
dgn-np:NP11753.RAqhubQ14A-512VnJsQgQLEwShqdvvurQW6pQGgtYGysk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP11753.RAqhubQ14A-512VnJsQgQLEwShqdvvurQW6pQGgtYGysk130_assertion
{
miriam-gene:11200
a
ncit:C16612
.
lld:C0029463
a
ncit:C7057
.
dgn-gda:DGNaebba282d872747518916a5ea3c4e2b2
sio:SIO_000628
miriam-gene:11200
,
lld:C0029463
;
a
sio:SIO_001121
.
}
dgn-np:NP11753.RAqhubQ14A-512VnJsQgQLEwShqdvvurQW6pQGgtYGysk130_provenance
{
dgn-np:NP11753.RAqhubQ14A-512VnJsQgQLEwShqdvvurQW6pQGgtYGysk130_assertion
dcterms:description
"[Exploiting the genomic sequence of chromosome 22, we looked for mutations in the exons and intron junctions of the CHK2 gene in DNA samples from 170 patients (57 osteosarcomas, 25 other sarcomas, 35 nonsmall-cell lung, 20 ovarian, and 33 breast cancers).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
wi:evidence
dgn-void:source_evidence_curated
;
sio:SIO_000772
miriam-pubmed:11746983
;
prov:wasDerivedFrom
dgn-void:ctd_human-20130708
;
prov:wasGeneratedBy
eco:ECO_0000218
.
dgn-void:ctd_human-20130708
pav:importedOn
"2013-07-24"^^
xsd:date
.
dgn-void:source_evidence_curated
a
eco:ECO_0000205
;
rdfs:comment
"Gene-disease associations manually curated."@en ;
rdfs:label
"DisGeNET evidence - CURATED"@en .
}
dgn-np:NP11753.RAqhubQ14A-512VnJsQgQLEwShqdvvurQW6pQGgtYGysk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:03+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" .
}