@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP444134.RAIGTc5eeSLsGWRAcSOBd-EjfR8ujQNM2aJ9GqfSdVnbw
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP444134.RAIGTc5eeSLsGWRAcSOBd-EjfR8ujQNM2aJ9GqfSdVnbw130_assertion
;
np:hasProvenance
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dgn-np:NP444134.RAIGTc5eeSLsGWRAcSOBd-EjfR8ujQNM2aJ9GqfSdVnbw130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP444134.RAIGTc5eeSLsGWRAcSOBd-EjfR8ujQNM2aJ9GqfSdVnbw130_assertion
a
np:Assertion
.
dgn-np:NP444134.RAIGTc5eeSLsGWRAcSOBd-EjfR8ujQNM2aJ9GqfSdVnbw130_provenance
a
np:Provenance
.
dgn-np:NP444134.RAIGTc5eeSLsGWRAcSOBd-EjfR8ujQNM2aJ9GqfSdVnbw130_publicationInfo
a
np:PublicationInfo
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dgn-np:NP444134.RAIGTc5eeSLsGWRAcSOBd-EjfR8ujQNM2aJ9GqfSdVnbw130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C1707446
a
ncit:C7057
.
dgn-gda:DGN23baf855c7a3a58f2fd8d0a90c1e1f87
sio:SIO_000628
miriam-gene:5979
,
lld:C1707446
;
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.
}
dgn-np:NP444134.RAIGTc5eeSLsGWRAcSOBd-EjfR8ujQNM2aJ9GqfSdVnbw130_provenance
{
dgn-np:NP444134.RAIGTc5eeSLsGWRAcSOBd-EjfR8ujQNM2aJ9GqfSdVnbw130_assertion
dcterms:description
"[We suggest that prophylactic thyroidectomy should not be delayed until adulthood in MEN 2A families carrying codon 804 RET mutations, but should be performed when there is CCH, before the development of MTC, as close as possible to age 6 years, which is the age of the youngest reported case of MTC in '804' families.]. 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:16343097
;
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:NP444134.RAIGTc5eeSLsGWRAcSOBd-EjfR8ujQNM2aJ9GqfSdVnbw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:25+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
<
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> , <
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> , <
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
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pav:version
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