@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ
> .
@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:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_head
{
this:
np:hasAssertion
dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_assertion
;
np:hasProvenance
dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_assertion
a
np:Assertion
.
dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_provenance
a
np:Provenance
.
dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0030521
a
ncit:C7057
.
dgn-gda:DGN665fbd597e2dfd2ea5c14e29c35e6b0e
sio:SIO_000628
miriam-gene:3342
,
lld:C0030521
;
a
sio:SIO_001121
.
}
dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_provenance
{
dgn-np:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_assertion
dcterms:description
"[For this purpose, nine parathyroid tumors with established CDC73 gene inactivating mutations (three carcinomas, one atypical adenoma and five adenomas) were analyzed for copy number alterations and loss of heterozygosity using array-comparative genomic hybridization (a-CGH) and single nucleotide polymorphism (SNP) microarrays, respectively.]. 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:23029479
;
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:NP685476.RAg09qsvRw6vQAPxC-mtvKRp0iLDsHPgmJk5yptUbjmCQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:56+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" .
}