@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP531589.RAK0fxwFRJPs6Y1dfnNXg2vsM1JM_3LQmqQkm8IEKEjpk
> .
@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:NP531589.RAK0fxwFRJPs6Y1dfnNXg2vsM1JM_3LQmqQkm8IEKEjpk130_head
{
this:
np:hasAssertion
dgn-np:NP531589.RAK0fxwFRJPs6Y1dfnNXg2vsM1JM_3LQmqQkm8IEKEjpk130_assertion
;
np:hasProvenance
dgn-np:NP531589.RAK0fxwFRJPs6Y1dfnNXg2vsM1JM_3LQmqQkm8IEKEjpk130_provenance
;
np:hasPublicationInfo
dgn-np:NP531589.RAK0fxwFRJPs6Y1dfnNXg2vsM1JM_3LQmqQkm8IEKEjpk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP531589.RAK0fxwFRJPs6Y1dfnNXg2vsM1JM_3LQmqQkm8IEKEjpk130_assertion
a
np:Assertion
.
dgn-np:NP531589.RAK0fxwFRJPs6Y1dfnNXg2vsM1JM_3LQmqQkm8IEKEjpk130_provenance
a
np:Provenance
.
dgn-np:NP531589.RAK0fxwFRJPs6Y1dfnNXg2vsM1JM_3LQmqQkm8IEKEjpk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP531589.RAK0fxwFRJPs6Y1dfnNXg2vsM1JM_3LQmqQkm8IEKEjpk130_assertion
{
miriam-gene:10573
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN8242eafd28b2c7825e04cea70f70b63b
sio:SIO_000628
miriam-gene:10573
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP531589.RAK0fxwFRJPs6Y1dfnNXg2vsM1JM_3LQmqQkm8IEKEjpk130_provenance
{
dgn-np:NP531589.RAK0fxwFRJPs6Y1dfnNXg2vsM1JM_3LQmqQkm8IEKEjpk130_assertion
dcterms:description
"[As PCR based approaches analyzing for homozygous deletions could be confounded by unavoidable contributions of normal cells in microdissected tissue, we performed in situ hybridization (ISH) on primary prostate carcinomas to accurately evaluate p16 and p15 copy numbers on a cell-by-cell basis.]. 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:11025389
;
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:NP531589.RAK0fxwFRJPs6Y1dfnNXg2vsM1JM_3LQmqQkm8IEKEjpk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:21+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" .
}