@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP552726.RA3vLW-HGwtHK8n9FqCH8oskown4nZByDAvoyWLQxAMPs
> .
@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:NP552726.RA3vLW-HGwtHK8n9FqCH8oskown4nZByDAvoyWLQxAMPs130_head
{
this:
np:hasAssertion
dgn-np:NP552726.RA3vLW-HGwtHK8n9FqCH8oskown4nZByDAvoyWLQxAMPs130_assertion
;
np:hasProvenance
dgn-np:NP552726.RA3vLW-HGwtHK8n9FqCH8oskown4nZByDAvoyWLQxAMPs130_provenance
;
np:hasPublicationInfo
dgn-np:NP552726.RA3vLW-HGwtHK8n9FqCH8oskown4nZByDAvoyWLQxAMPs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP552726.RA3vLW-HGwtHK8n9FqCH8oskown4nZByDAvoyWLQxAMPs130_assertion
a
np:Assertion
.
dgn-np:NP552726.RA3vLW-HGwtHK8n9FqCH8oskown4nZByDAvoyWLQxAMPs130_provenance
a
np:Provenance
.
dgn-np:NP552726.RA3vLW-HGwtHK8n9FqCH8oskown4nZByDAvoyWLQxAMPs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP552726.RA3vLW-HGwtHK8n9FqCH8oskown4nZByDAvoyWLQxAMPs130_assertion
{
miriam-gene:595
a
ncit:C16612
.
lld:C0030521
a
ncit:C7057
.
dgn-gda:DGNfdff9e968cb74c27021e46a651c2386e
sio:SIO_000628
miriam-gene:595
,
lld:C0030521
;
a
sio:SIO_001121
.
}
dgn-np:NP552726.RA3vLW-HGwtHK8n9FqCH8oskown4nZByDAvoyWLQxAMPs130_provenance
{
dgn-np:NP552726.RA3vLW-HGwtHK8n9FqCH8oskown4nZByDAvoyWLQxAMPs130_assertion
dcterms:description
"[Only one oncogene, cyclin D1/PRAD1, has an established role in parathyroid tumorigenesis, and parathyroid tumor suppressor genes on chromosome arms 1p and 11q, which still have not been identified, have also been implicated by loss of heterozygosity analysis.]. 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:8564978
;
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:NP552726.RA3vLW-HGwtHK8n9FqCH8oskown4nZByDAvoyWLQxAMPs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:33+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" .
}