@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA
> .
@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:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_head
{
this:
np:hasAssertion
dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_assertion
;
np:hasProvenance
dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_provenance
;
np:hasPublicationInfo
dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_assertion
a
np:Assertion
.
dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_provenance
a
np:Provenance
.
dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0023055
a
ncit:C7057
.
dgn-gda:DGN8b505477d5e15a04f05de1c4a226a07e
sio:SIO_000628
miriam-gene:3342
,
lld:C0023055
;
a
sio:SIO_001121
.
}
dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_provenance
{
dgn-np:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_assertion
dcterms:description
"[Our recent comparative genomic hybridization (CGH) study has shown that losses of the long arm of chromosome 13 were the most common aberrations in primary larynx tumors and their corresponding metastases.]. 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:12377414
;
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:NP646812.RAgw1GvAxNvqOpPRvAA2WnjHTa2lmVAHSlJ_s-SxJPGSA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:29+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" .
}