@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP412682.RAy_bcZrNYy4xdF-Qq1oRRnpI9x0ykg4aABdQ4-5-75k4
> .
@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:NP412682.RAy_bcZrNYy4xdF-Qq1oRRnpI9x0ykg4aABdQ4-5-75k4130_head
{
this:
np:hasAssertion
dgn-np:NP412682.RAy_bcZrNYy4xdF-Qq1oRRnpI9x0ykg4aABdQ4-5-75k4130_assertion
;
np:hasProvenance
dgn-np:NP412682.RAy_bcZrNYy4xdF-Qq1oRRnpI9x0ykg4aABdQ4-5-75k4130_provenance
;
np:hasPublicationInfo
dgn-np:NP412682.RAy_bcZrNYy4xdF-Qq1oRRnpI9x0ykg4aABdQ4-5-75k4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP412682.RAy_bcZrNYy4xdF-Qq1oRRnpI9x0ykg4aABdQ4-5-75k4130_assertion
a
np:Assertion
.
dgn-np:NP412682.RAy_bcZrNYy4xdF-Qq1oRRnpI9x0ykg4aABdQ4-5-75k4130_provenance
a
np:Provenance
.
dgn-np:NP412682.RAy_bcZrNYy4xdF-Qq1oRRnpI9x0ykg4aABdQ4-5-75k4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP412682.RAy_bcZrNYy4xdF-Qq1oRRnpI9x0ykg4aABdQ4-5-75k4130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0017638
a
ncit:C7057
.
dgn-gda:DGN08c827d24aea305561d6fcbe13b35520
sio:SIO_000628
miriam-gene:7248
,
lld:C0017638
;
a
sio:SIO_001121
.
}
dgn-np:NP412682.RAy_bcZrNYy4xdF-Qq1oRRnpI9x0ykg4aABdQ4-5-75k4130_provenance
{
dgn-np:NP412682.RAy_bcZrNYy4xdF-Qq1oRRnpI9x0ykg4aABdQ4-5-75k4130_assertion
dcterms:description
"[A microsatellite-based marker set is used to detect the deletion status of genomic regions (i) with established diagnostic relevance, (ii) recurrently found deleted in gliomas, or (iii) generally associated with tumour suppressor activity.]. 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:15259374
;
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:NP412682.RAy_bcZrNYy4xdF-Qq1oRRnpI9x0ykg4aABdQ4-5-75k4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:05+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" .
}