@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP190422.RADMOAzykzu0pItqffIwBe8bIWwJ17VXwy9ULQTK2b4ls
> .
@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:NP190422.RADMOAzykzu0pItqffIwBe8bIWwJ17VXwy9ULQTK2b4ls130_head
{
this:
np:hasAssertion
dgn-np:NP190422.RADMOAzykzu0pItqffIwBe8bIWwJ17VXwy9ULQTK2b4ls130_assertion
;
np:hasProvenance
dgn-np:NP190422.RADMOAzykzu0pItqffIwBe8bIWwJ17VXwy9ULQTK2b4ls130_provenance
;
np:hasPublicationInfo
dgn-np:NP190422.RADMOAzykzu0pItqffIwBe8bIWwJ17VXwy9ULQTK2b4ls130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP190422.RADMOAzykzu0pItqffIwBe8bIWwJ17VXwy9ULQTK2b4ls130_assertion
a
np:Assertion
.
dgn-np:NP190422.RADMOAzykzu0pItqffIwBe8bIWwJ17VXwy9ULQTK2b4ls130_provenance
a
np:Provenance
.
dgn-np:NP190422.RADMOAzykzu0pItqffIwBe8bIWwJ17VXwy9ULQTK2b4ls130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP190422.RADMOAzykzu0pItqffIwBe8bIWwJ17VXwy9ULQTK2b4ls130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0238462
a
ncit:C7057
.
dgn-gda:DGNff556bef512bb50a165bdf940313814e
sio:SIO_000628
miriam-gene:5979
,
lld:C0238462
;
a
sio:SIO_001121
.
}
dgn-np:NP190422.RADMOAzykzu0pItqffIwBe8bIWwJ17VXwy9ULQTK2b4ls130_provenance
{
dgn-np:NP190422.RADMOAzykzu0pItqffIwBe8bIWwJ17VXwy9ULQTK2b4ls130_assertion
dcterms:description
"[Despite variable penetrance, each carrier of a RET protooncogene germline mutation should undergo thyroidectomy, even if basal and stimulated calcitonin levels are normal because at present no test can exclude or predict the age of development of 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:12205548
;
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:NP190422.RADMOAzykzu0pItqffIwBe8bIWwJ17VXwy9ULQTK2b4ls130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:44+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" .
}