@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP627816.RAgGhZPxXKpdnqZWkZmZapStG2Utf8Kf7nKnU3-24oVqw
> .
@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:NP627816.RAgGhZPxXKpdnqZWkZmZapStG2Utf8Kf7nKnU3-24oVqw130_head
{
this:
np:hasAssertion
dgn-np:NP627816.RAgGhZPxXKpdnqZWkZmZapStG2Utf8Kf7nKnU3-24oVqw130_assertion
;
np:hasProvenance
dgn-np:NP627816.RAgGhZPxXKpdnqZWkZmZapStG2Utf8Kf7nKnU3-24oVqw130_provenance
;
np:hasPublicationInfo
dgn-np:NP627816.RAgGhZPxXKpdnqZWkZmZapStG2Utf8Kf7nKnU3-24oVqw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP627816.RAgGhZPxXKpdnqZWkZmZapStG2Utf8Kf7nKnU3-24oVqw130_assertion
a
np:Assertion
.
dgn-np:NP627816.RAgGhZPxXKpdnqZWkZmZapStG2Utf8Kf7nKnU3-24oVqw130_provenance
a
np:Provenance
.
dgn-np:NP627816.RAgGhZPxXKpdnqZWkZmZapStG2Utf8Kf7nKnU3-24oVqw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP627816.RAgGhZPxXKpdnqZWkZmZapStG2Utf8Kf7nKnU3-24oVqw130_assertion
{
miriam-gene:7248
a
ncit:C16612
.
lld:C1861305
a
ncit:C7057
.
dgn-gda:DGN49263f00b795fb52ecde71cf78c8845e
sio:SIO_000628
miriam-gene:7248
,
lld:C1861305
;
a
sio:SIO_001121
.
}
dgn-np:NP627816.RAgGhZPxXKpdnqZWkZmZapStG2Utf8Kf7nKnU3-24oVqw130_provenance
{
dgn-np:NP627816.RAgGhZPxXKpdnqZWkZmZapStG2Utf8Kf7nKnU3-24oVqw130_assertion
dcterms:description
"[Chromosome 9q deletion is frequently found in transitional cell carcinoma (TCC) of the bladder and upper urinary tract and one of the putative tumour suppressor loci has been mapped to 9q32-33.]. 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:11313984
;
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:NP627816.RAgGhZPxXKpdnqZWkZmZapStG2Utf8Kf7nKnU3-24oVqw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:19+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" .
}