@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP226127.RA2VDqF-xxNyjDwibZ72a0DqE4mXswwGISUGysIif-PT0
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP226127.RA2VDqF-xxNyjDwibZ72a0DqE4mXswwGISUGysIif-PT0130_assertion
;
np:hasProvenance
dgn-np:NP226127.RA2VDqF-xxNyjDwibZ72a0DqE4mXswwGISUGysIif-PT0130_provenance
;
np:hasPublicationInfo
dgn-np:NP226127.RA2VDqF-xxNyjDwibZ72a0DqE4mXswwGISUGysIif-PT0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP226127.RA2VDqF-xxNyjDwibZ72a0DqE4mXswwGISUGysIif-PT0130_assertion
a
np:Assertion
.
dgn-np:NP226127.RA2VDqF-xxNyjDwibZ72a0DqE4mXswwGISUGysIif-PT0130_provenance
a
np:Provenance
.
dgn-np:NP226127.RA2VDqF-xxNyjDwibZ72a0DqE4mXswwGISUGysIif-PT0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP226127.RA2VDqF-xxNyjDwibZ72a0DqE4mXswwGISUGysIif-PT0130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0007138
a
ncit:C7057
.
dgn-gda:DGN4fb393f98aefd8cdb21ae1236d4e2e4f
sio:SIO_000628
miriam-gene:7157
,
lld:C0007138
;
a
sio:SIO_001121
.
}
dgn-np:NP226127.RA2VDqF-xxNyjDwibZ72a0DqE4mXswwGISUGysIif-PT0130_provenance
{
dgn-np:NP226127.RA2VDqF-xxNyjDwibZ72a0DqE4mXswwGISUGysIif-PT0130_assertion
dcterms:description
"[Loss of heterozygosity (LOH) assays for 3 microsatellite polymorphic markers on chromosome 9p21 (D9S171, region of putative tumor suppressor gene p16), 9q32 (D9S177, putative tumor suppressor gene involved in urothelial carcinoma tumorigenesis), and 17p13 (TP53, the p53 locus) were performed.]. 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:16196038
;
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:NP226127.RA2VDqF-xxNyjDwibZ72a0DqE4mXswwGISUGysIif-PT0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:05+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" .
}