@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP860016.RAnAZNGZuScVHAx2AYrWhy8njl1LG4FuH-LjE1HRXl7zE
> .
@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:NP860016.RAnAZNGZuScVHAx2AYrWhy8njl1LG4FuH-LjE1HRXl7zE130_head
{
this:
np:hasAssertion
dgn-np:NP860016.RAnAZNGZuScVHAx2AYrWhy8njl1LG4FuH-LjE1HRXl7zE130_assertion
;
np:hasProvenance
dgn-np:NP860016.RAnAZNGZuScVHAx2AYrWhy8njl1LG4FuH-LjE1HRXl7zE130_provenance
;
np:hasPublicationInfo
dgn-np:NP860016.RAnAZNGZuScVHAx2AYrWhy8njl1LG4FuH-LjE1HRXl7zE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP860016.RAnAZNGZuScVHAx2AYrWhy8njl1LG4FuH-LjE1HRXl7zE130_assertion
a
np:Assertion
.
dgn-np:NP860016.RAnAZNGZuScVHAx2AYrWhy8njl1LG4FuH-LjE1HRXl7zE130_provenance
a
np:Provenance
.
dgn-np:NP860016.RAnAZNGZuScVHAx2AYrWhy8njl1LG4FuH-LjE1HRXl7zE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP860016.RAnAZNGZuScVHAx2AYrWhy8njl1LG4FuH-LjE1HRXl7zE130_assertion
{
miriam-gene:1871
a
ncit:C16612
.
lld:C0035335
a
ncit:C7057
.
dgn-gda:DGN11eb27bf8bfc5435674adc15f0faa332
sio:SIO_000628
miriam-gene:1871
,
lld:C0035335
;
a
sio:SIO_001121
.
}
dgn-np:NP860016.RAnAZNGZuScVHAx2AYrWhy8njl1LG4FuH-LjE1HRXl7zE130_provenance
{
dgn-np:NP860016.RAnAZNGZuScVHAx2AYrWhy8njl1LG4FuH-LjE1HRXl7zE130_assertion
dcterms:description
"[Gene-specific quantitative multiplex polymerase chain reaction of candidate oncogenes at 1q32.1 (KIF14), 6p22 (E2F3 and DEK), and tumor suppressor genes at 16q22 (CDH11) and 17q21 (NGFR) showed the most common gene gains in RB to be KIF14 in cell lines (80%) and E2F3 in primary tumors (70%).]. 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:17099872
;
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:NP860016.RAnAZNGZuScVHAx2AYrWhy8njl1LG4FuH-LjE1HRXl7zE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:45+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" .
}