@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP551610.RAjafA3vm-R5qK2_pPUXKY2sFAk6EFqj1_P95Sv5kL_YQ
> .
@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:NP551610.RAjafA3vm-R5qK2_pPUXKY2sFAk6EFqj1_P95Sv5kL_YQ130_head
{
this:
np:hasAssertion
dgn-np:NP551610.RAjafA3vm-R5qK2_pPUXKY2sFAk6EFqj1_P95Sv5kL_YQ130_assertion
;
np:hasProvenance
dgn-np:NP551610.RAjafA3vm-R5qK2_pPUXKY2sFAk6EFqj1_P95Sv5kL_YQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP551610.RAjafA3vm-R5qK2_pPUXKY2sFAk6EFqj1_P95Sv5kL_YQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP551610.RAjafA3vm-R5qK2_pPUXKY2sFAk6EFqj1_P95Sv5kL_YQ130_assertion
a
np:Assertion
.
dgn-np:NP551610.RAjafA3vm-R5qK2_pPUXKY2sFAk6EFqj1_P95Sv5kL_YQ130_provenance
a
np:Provenance
.
dgn-np:NP551610.RAjafA3vm-R5qK2_pPUXKY2sFAk6EFqj1_P95Sv5kL_YQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP551610.RAjafA3vm-R5qK2_pPUXKY2sFAk6EFqj1_P95Sv5kL_YQ130_assertion
{
miriam-gene:367
a
ncit:C16612
.
lld:C0025268
a
ncit:C7057
.
dgn-gda:DGN47e9d180e47b7bd3209cdbd952dfdeef
sio:SIO_000628
miriam-gene:367
,
lld:C0025268
;
a
sio:SIO_001121
.
}
dgn-np:NP551610.RAjafA3vm-R5qK2_pPUXKY2sFAk6EFqj1_P95Sv5kL_YQ130_provenance
{
dgn-np:NP551610.RAjafA3vm-R5qK2_pPUXKY2sFAk6EFqj1_P95Sv5kL_YQ130_assertion
dcterms:description
"[To test this hypothesis, we examined thyroid tissue from 27 consecutive autopsy cases for the presence of CCH (defined as >50 C-cells/x100 magnification in three fields) and for AR expression in autopsy cases and in 43 medullary thyroid carcinomas (MTCs) from patients with sporadic and familial disease as well as two multiple endocrine neoplasia type 2A patients with only CCH.]. 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:12858007
;
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:NP551610.RAjafA3vm-R5qK2_pPUXKY2sFAk6EFqj1_P95Sv5kL_YQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:32+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" .
}