@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY
> .
@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:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_head
{
this:
np:hasAssertion
dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_assertion
;
np:hasProvenance
dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_provenance
;
np:hasPublicationInfo
dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_assertion
a
np:Assertion
.
dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_provenance
a
np:Provenance
.
dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_assertion
{
miriam-gene:3342
a
ncit:C16612
.
lld:C0030521
a
ncit:C7057
.
dgn-gda:DGNfe6b2c4ae1337e930936b3166fd7598c
sio:SIO_000628
miriam-gene:3342
,
lld:C0030521
;
a
sio:SIO_001121
.
}
dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_provenance
{
dgn-np:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_assertion
dcterms:description
"[Most of the information about the genetic composition of parathyroid tumors has been obtained by comparative genomic hybridization (CGH) and loss of heterozygosity (LOH) studies, whereas only few conventional cytogenetic investigation results are available.]. 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:17455879
;
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:NP831635.RAEFRdxZTCb6X_8OPbbS-afUY2cxQ5gcv6dQkdHVNt1oY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:29+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" .
}