@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP731115.RAyAUH4DtDTQUugLwOjiyzzUuEeppiXI27QYRHOA6wM8Y
> .
@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:NP731115.RAyAUH4DtDTQUugLwOjiyzzUuEeppiXI27QYRHOA6wM8Y130_head
{
this:
np:hasAssertion
dgn-np:NP731115.RAyAUH4DtDTQUugLwOjiyzzUuEeppiXI27QYRHOA6wM8Y130_assertion
;
np:hasProvenance
dgn-np:NP731115.RAyAUH4DtDTQUugLwOjiyzzUuEeppiXI27QYRHOA6wM8Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP731115.RAyAUH4DtDTQUugLwOjiyzzUuEeppiXI27QYRHOA6wM8Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP731115.RAyAUH4DtDTQUugLwOjiyzzUuEeppiXI27QYRHOA6wM8Y130_assertion
a
np:Assertion
.
dgn-np:NP731115.RAyAUH4DtDTQUugLwOjiyzzUuEeppiXI27QYRHOA6wM8Y130_provenance
a
np:Provenance
.
dgn-np:NP731115.RAyAUH4DtDTQUugLwOjiyzzUuEeppiXI27QYRHOA6wM8Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP731115.RAyAUH4DtDTQUugLwOjiyzzUuEeppiXI27QYRHOA6wM8Y130_assertion
{
miriam-gene:57045
a
ncit:C16612
.
lld:C0007137
a
ncit:C7057
.
dgn-gda:DGNccaa57a751fb86b5ba3efafa31a4575a
sio:SIO_000628
miriam-gene:57045
,
lld:C0007137
;
a
sio:SIO_001121
.
}
dgn-np:NP731115.RAyAUH4DtDTQUugLwOjiyzzUuEeppiXI27QYRHOA6wM8Y130_provenance
{
dgn-np:NP731115.RAyAUH4DtDTQUugLwOjiyzzUuEeppiXI27QYRHOA6wM8Y130_assertion
dcterms:description
"[To investigate area susceptible to harbor TSG(s) involved in OSCC on 1p36 region, paired normal and tumor tissues of 27 patients with diagnosis of OSCC have been analyzed for loss of heterozygosity (LOH) using nine microsatellite markers based on recent gene mapping.]. 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:18363675
;
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:NP731115.RAyAUH4DtDTQUugLwOjiyzzUuEeppiXI27QYRHOA6wM8Y130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:23+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" .
}