@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP818883.RAttIafYX_aLaNMXcnWN0J1dD4kA01Z6k8ap85ExqLkUc
> .
@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:NP818883.RAttIafYX_aLaNMXcnWN0J1dD4kA01Z6k8ap85ExqLkUc130_head
{
this:
np:hasAssertion
dgn-np:NP818883.RAttIafYX_aLaNMXcnWN0J1dD4kA01Z6k8ap85ExqLkUc130_assertion
;
np:hasProvenance
dgn-np:NP818883.RAttIafYX_aLaNMXcnWN0J1dD4kA01Z6k8ap85ExqLkUc130_provenance
;
np:hasPublicationInfo
dgn-np:NP818883.RAttIafYX_aLaNMXcnWN0J1dD4kA01Z6k8ap85ExqLkUc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP818883.RAttIafYX_aLaNMXcnWN0J1dD4kA01Z6k8ap85ExqLkUc130_assertion
a
np:Assertion
.
dgn-np:NP818883.RAttIafYX_aLaNMXcnWN0J1dD4kA01Z6k8ap85ExqLkUc130_provenance
a
np:Provenance
.
dgn-np:NP818883.RAttIafYX_aLaNMXcnWN0J1dD4kA01Z6k8ap85ExqLkUc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP818883.RAttIafYX_aLaNMXcnWN0J1dD4kA01Z6k8ap85ExqLkUc130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C0025286
a
ncit:C7057
.
dgn-gda:DGN8eab239e922b6a0947d895cc575a32d7
sio:SIO_000628
miriam-gene:7248
,
lld:C0025286
;
a
sio:SIO_001121
.
}
dgn-np:NP818883.RAttIafYX_aLaNMXcnWN0J1dD4kA01Z6k8ap85ExqLkUc130_provenance
{
dgn-np:NP818883.RAttIafYX_aLaNMXcnWN0J1dD4kA01Z6k8ap85ExqLkUc130_assertion
dcterms:description
"[The minimal deletion common to 81 meningiomas, and thus the position of the tentative meningioma tumour suppressor gene (TSG), has been determined to lie distal to the myoglobin locus on the long arm of chromosome 22, corresponding to the region 22q12.3-qter.]. 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:1688296
;
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:NP818883.RAttIafYX_aLaNMXcnWN0J1dD4kA01Z6k8ap85ExqLkUc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:21+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" .
}