@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP991572.RAMgCFxw2I-zXs4nskGgwdaYA_gIilj4OEtGkz69yOiNM
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP991572.RAMgCFxw2I-zXs4nskGgwdaYA_gIilj4OEtGkz69yOiNM130_head
{
this:
np:hasAssertion
dgn-np:NP991572.RAMgCFxw2I-zXs4nskGgwdaYA_gIilj4OEtGkz69yOiNM130_assertion
;
np:hasProvenance
dgn-np:NP991572.RAMgCFxw2I-zXs4nskGgwdaYA_gIilj4OEtGkz69yOiNM130_provenance
;
np:hasPublicationInfo
dgn-np:NP991572.RAMgCFxw2I-zXs4nskGgwdaYA_gIilj4OEtGkz69yOiNM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP991572.RAMgCFxw2I-zXs4nskGgwdaYA_gIilj4OEtGkz69yOiNM130_assertion
a
np:Assertion
.
dgn-np:NP991572.RAMgCFxw2I-zXs4nskGgwdaYA_gIilj4OEtGkz69yOiNM130_provenance
a
np:Provenance
.
dgn-np:NP991572.RAMgCFxw2I-zXs4nskGgwdaYA_gIilj4OEtGkz69yOiNM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP991572.RAMgCFxw2I-zXs4nskGgwdaYA_gIilj4OEtGkz69yOiNM130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0025268
a
ncit:C7057
.
dgn-gda:DGN714db87b42d8e50868f2ce0c8b5de6d2
sio:SIO_000628
miriam-gene:5979
,
lld:C0025268
;
a
sio:SIO_001121
.
}
dgn-np:NP991572.RAMgCFxw2I-zXs4nskGgwdaYA_gIilj4OEtGkz69yOiNM130_provenance
{
dgn-np:NP991572.RAMgCFxw2I-zXs4nskGgwdaYA_gIilj4OEtGkz69yOiNM130_assertion
dcterms:description
"[Multiple endocrine neoplasia 2a (MEN2a) syndrome is one of the rare genetic disorder where prophylactic thyroidectomy is recommended for RET mutation carriers due to increased risk for developing MTC during lifetime.]. 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:22715565
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP991572.RAMgCFxw2I-zXs4nskGgwdaYA_gIilj4OEtGkz69yOiNM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:15+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}