@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP283175.RAtmgX6KbXAGpG6XjwkGGqD_VrBftGF7s7rRQ5JLm1HvI
> .
@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:NP283175.RAtmgX6KbXAGpG6XjwkGGqD_VrBftGF7s7rRQ5JLm1HvI130_head
{
this:
np:hasAssertion
dgn-np:NP283175.RAtmgX6KbXAGpG6XjwkGGqD_VrBftGF7s7rRQ5JLm1HvI130_assertion
;
np:hasProvenance
dgn-np:NP283175.RAtmgX6KbXAGpG6XjwkGGqD_VrBftGF7s7rRQ5JLm1HvI130_provenance
;
np:hasPublicationInfo
dgn-np:NP283175.RAtmgX6KbXAGpG6XjwkGGqD_VrBftGF7s7rRQ5JLm1HvI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP283175.RAtmgX6KbXAGpG6XjwkGGqD_VrBftGF7s7rRQ5JLm1HvI130_assertion
a
np:Assertion
.
dgn-np:NP283175.RAtmgX6KbXAGpG6XjwkGGqD_VrBftGF7s7rRQ5JLm1HvI130_provenance
a
np:Provenance
.
dgn-np:NP283175.RAtmgX6KbXAGpG6XjwkGGqD_VrBftGF7s7rRQ5JLm1HvI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP283175.RAtmgX6KbXAGpG6XjwkGGqD_VrBftGF7s7rRQ5JLm1HvI130_assertion
{
miriam-gene:1029
a
ncit:C16612
.
lld:C0178874
a
ncit:C7057
.
dgn-gda:DGN666291a18c39df6172d534431e9bf462
sio:SIO_000628
miriam-gene:1029
,
lld:C0178874
;
a
sio:SIO_001121
.
}
dgn-np:NP283175.RAtmgX6KbXAGpG6XjwkGGqD_VrBftGF7s7rRQ5JLm1HvI130_provenance
{
dgn-np:NP283175.RAtmgX6KbXAGpG6XjwkGGqD_VrBftGF7s7rRQ5JLm1HvI130_assertion
dcterms:description
"[We determined the prevalence of allelic loss at 9p21 and mutations in CDKN2 in esophageal adenocarcinomas and investigated the order in which they occurred relative to the development of aneuploidy and cancer during neoplastic progression.]. 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:8934532
;
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:NP283175.RAtmgX6KbXAGpG6XjwkGGqD_VrBftGF7s7rRQ5JLm1HvI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:39+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" .
}