@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP288131.RAFBxpv4m79Arx3nHEGdY80T78zWn4OQ3JF6Oq-mX8jXY
> .
@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:NP288131.RAFBxpv4m79Arx3nHEGdY80T78zWn4OQ3JF6Oq-mX8jXY130_head
{
this:
np:hasAssertion
dgn-np:NP288131.RAFBxpv4m79Arx3nHEGdY80T78zWn4OQ3JF6Oq-mX8jXY130_assertion
;
np:hasProvenance
dgn-np:NP288131.RAFBxpv4m79Arx3nHEGdY80T78zWn4OQ3JF6Oq-mX8jXY130_provenance
;
np:hasPublicationInfo
dgn-np:NP288131.RAFBxpv4m79Arx3nHEGdY80T78zWn4OQ3JF6Oq-mX8jXY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP288131.RAFBxpv4m79Arx3nHEGdY80T78zWn4OQ3JF6Oq-mX8jXY130_assertion
a
np:Assertion
.
dgn-np:NP288131.RAFBxpv4m79Arx3nHEGdY80T78zWn4OQ3JF6Oq-mX8jXY130_provenance
a
np:Provenance
.
dgn-np:NP288131.RAFBxpv4m79Arx3nHEGdY80T78zWn4OQ3JF6Oq-mX8jXY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP288131.RAFBxpv4m79Arx3nHEGdY80T78zWn4OQ3JF6Oq-mX8jXY130_assertion
{
miriam-gene:4292
a
ncit:C16612
.
lld:C0007138
a
ncit:C7057
.
dgn-gda:DGNfcdef986947266f99b72d1141356de7a
sio:SIO_000628
miriam-gene:4292
,
lld:C0007138
;
a
sio:SIO_001121
.
}
dgn-np:NP288131.RAFBxpv4m79Arx3nHEGdY80T78zWn4OQ3JF6Oq-mX8jXY130_provenance
{
dgn-np:NP288131.RAFBxpv4m79Arx3nHEGdY80T78zWn4OQ3JF6Oq-mX8jXY130_assertion
dcterms:description
"[Low-grade dysplasia (18) and carcinoma in situ (12) associated with muscle-invasive urothelial carcinoma were microdissected and topographically analyzed (intraepithelial and invasive superficial and deep to muscularis mucosa) for methylation pattern of androgen receptor alleles, TP53, RB1, WT1, and NF1 microsatellite analysis to assess clonal identity; MLH1 and MSH2 sequencing/immunostaining.]. 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:19368958
;
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:NP288131.RAFBxpv4m79Arx3nHEGdY80T78zWn4OQ3JF6Oq-mX8jXY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:44+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" .
}