@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP663199.RA_iSvAJf_5JmIqM9v6nc01_wQyD9dEFDtMewxoh3L1Rw
> .
@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:NP663199.RA_iSvAJf_5JmIqM9v6nc01_wQyD9dEFDtMewxoh3L1Rw130_head
{
this:
np:hasAssertion
dgn-np:NP663199.RA_iSvAJf_5JmIqM9v6nc01_wQyD9dEFDtMewxoh3L1Rw130_assertion
;
np:hasProvenance
dgn-np:NP663199.RA_iSvAJf_5JmIqM9v6nc01_wQyD9dEFDtMewxoh3L1Rw130_provenance
;
np:hasPublicationInfo
dgn-np:NP663199.RA_iSvAJf_5JmIqM9v6nc01_wQyD9dEFDtMewxoh3L1Rw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP663199.RA_iSvAJf_5JmIqM9v6nc01_wQyD9dEFDtMewxoh3L1Rw130_assertion
a
np:Assertion
.
dgn-np:NP663199.RA_iSvAJf_5JmIqM9v6nc01_wQyD9dEFDtMewxoh3L1Rw130_provenance
a
np:Provenance
.
dgn-np:NP663199.RA_iSvAJf_5JmIqM9v6nc01_wQyD9dEFDtMewxoh3L1Rw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP663199.RA_iSvAJf_5JmIqM9v6nc01_wQyD9dEFDtMewxoh3L1Rw130_assertion
{
miriam-gene:9401
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGNe8bc1ec5fb5a114ca4d9284e1124e9aa
sio:SIO_000628
miriam-gene:9401
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP663199.RA_iSvAJf_5JmIqM9v6nc01_wQyD9dEFDtMewxoh3L1Rw130_provenance
{
dgn-np:NP663199.RA_iSvAJf_5JmIqM9v6nc01_wQyD9dEFDtMewxoh3L1Rw130_assertion
dcterms:description
"[Losses of CDKN2A (9p21) and MLH1 (3p22) and gains of CCND1, EMS1 (both at 11q13), RECQL4 and PTP4A3 (both at 8q24) were the most frequent aberrations in both larynx and pharynx carcinomas.]. 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:17641416
;
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:NP663199.RA_iSvAJf_5JmIqM9v6nc01_wQyD9dEFDtMewxoh3L1Rw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:40+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" .
}