@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP305396.RAJXF0e8qvSSQneWHWFQjuD_5Z6WxO6WLh00UNQyvmAiw
> .
@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:NP305396.RAJXF0e8qvSSQneWHWFQjuD_5Z6WxO6WLh00UNQyvmAiw130_head
{
this:
np:hasAssertion
dgn-np:NP305396.RAJXF0e8qvSSQneWHWFQjuD_5Z6WxO6WLh00UNQyvmAiw130_assertion
;
np:hasProvenance
dgn-np:NP305396.RAJXF0e8qvSSQneWHWFQjuD_5Z6WxO6WLh00UNQyvmAiw130_provenance
;
np:hasPublicationInfo
dgn-np:NP305396.RAJXF0e8qvSSQneWHWFQjuD_5Z6WxO6WLh00UNQyvmAiw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP305396.RAJXF0e8qvSSQneWHWFQjuD_5Z6WxO6WLh00UNQyvmAiw130_assertion
a
np:Assertion
.
dgn-np:NP305396.RAJXF0e8qvSSQneWHWFQjuD_5Z6WxO6WLh00UNQyvmAiw130_provenance
a
np:Provenance
.
dgn-np:NP305396.RAJXF0e8qvSSQneWHWFQjuD_5Z6WxO6WLh00UNQyvmAiw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP305396.RAJXF0e8qvSSQneWHWFQjuD_5Z6WxO6WLh00UNQyvmAiw130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C1955745
a
ncit:C7057
.
dgn-gda:DGN0ea21ec2127f6f23a46d6cbf0aab8916
sio:SIO_000628
miriam-gene:5979
,
lld:C1955745
;
a
sio:SIO_001121
.
}
dgn-np:NP305396.RAJXF0e8qvSSQneWHWFQjuD_5Z6WxO6WLh00UNQyvmAiw130_provenance
{
dgn-np:NP305396.RAJXF0e8qvSSQneWHWFQjuD_5Z6WxO6WLh00UNQyvmAiw130_assertion
dcterms:description
"[Since the discovery that germ-line mutations in the RET protooncogene are responsible for the multiple endocrine neoplasia (MEN) syndromes types 2A and 2B, prophylactic thyroidectomy has been recommended for MEN patients to prevent medullary thyroid carcinoma (MTC).]. 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:9516056
;
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:NP305396.RAJXF0e8qvSSQneWHWFQjuD_5Z6WxO6WLh00UNQyvmAiw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:55+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" .
}