@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY
> .
@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:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_head
{
this:
np:hasAssertion
dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_assertion
;
np:hasProvenance
dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_provenance
;
np:hasPublicationInfo
dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_assertion
a
np:Assertion
.
dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_provenance
a
np:Provenance
.
dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0700095
a
ncit:C7057
.
dgn-gda:DGNe4c0f82aab31f36a8033a94674656950
sio:SIO_000628
miriam-gene:1029
,
lld:C0700095
;
a
sio:SIO_001121
.
}
dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_provenance
{
dgn-np:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_assertion
dcterms:description
"[We previously reported that loss of heterozygosity (LOH) on chromosome 9p21 correlates with poor prognosis of neuroblastoma and the p16 gene is not expressed in approximately two thirds of neuroblastoma cell lines.]. 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:9872329
;
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:NP343401.RA7zHNTyo8tPBbI27ejKF1d3hz6tilWwWmlZvYOjGmNUY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:22+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" .
}