@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU
> .
@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:NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_head
{
this:
np:hasAssertion
dgn-np:NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_assertion
;
np:hasProvenance
dgn-np:NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_provenance
;
np:hasPublicationInfo
dgn-np:NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_assertion
a
np:Assertion
.
dgn-np:NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_provenance
a
np:Provenance
.
dgn-np:NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_assertion
{
miriam-gene:1030
a
ncit:C16612
.
lld:C0279626
a
ncit:C7057
.
dgn-gda:DGNb4812d49cbd8fa0f1e746de291e847c2
sio:SIO_000628
miriam-gene:1030
,
lld:C0279626
;
a
sio:SIO_001121
.
}
dgn-np:NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_provenance
{
dgn-np:NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_assertion
dcterms:description
"[Because previous studies have shown that loss of heterozygosity (LOH) is common on chromosome arm 9p in esophageal squamous cell carcinoma (ESCC) and that genetic alterations in CDKN2A and CDKN2B on 9p are also common, we sought to determine whether LOH and these genetic alterations are related.]. 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:14732922
;
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:NP796615.RADGEpvSaamxMTeIeVrvttIw9CG8LxjL7a90jPziAawKU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:09+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" .
}