@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP446396.RAhz-6_kSque5rw1uPByYWzmwa-wmH3wErARiNcdXtnLc
> .
@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/
> .
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{
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np:hasAssertion
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np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP446396.RAhz-6_kSque5rw1uPByYWzmwa-wmH3wErARiNcdXtnLc130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP446396.RAhz-6_kSque5rw1uPByYWzmwa-wmH3wErARiNcdXtnLc130_assertion
a
np:Assertion
.
dgn-np:NP446396.RAhz-6_kSque5rw1uPByYWzmwa-wmH3wErARiNcdXtnLc130_provenance
a
np:Provenance
.
dgn-np:NP446396.RAhz-6_kSque5rw1uPByYWzmwa-wmH3wErARiNcdXtnLc130_publicationInfo
a
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{
miriam-gene:5979
a
ncit:C16612
.
lld:C0027662
a
ncit:C7057
.
dgn-gda:DGNb528fb171d84277aea29eaf6a8bf8d14
sio:SIO_000628
miriam-gene:5979
,
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;
a
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.
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dgn-np:NP446396.RAhz-6_kSque5rw1uPByYWzmwa-wmH3wErARiNcdXtnLc130_provenance
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dgn-np:NP446396.RAhz-6_kSque5rw1uPByYWzmwa-wmH3wErARiNcdXtnLc130_assertion
dcterms:description
"[To this end, we performed microarray expression analysis on benign (pheochromocytomas) and malignant (medullary thyroid carcinomas, MTCs) tumors from patients with multiple endocrine neoplasia (MEN) type 2A or 2B, related syndromes that result from distinctive mutations in the RET receptor tyrosine kinase.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine."@en ;
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sio:SIO_000772
miriam-pubmed:15173001
;
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;
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 .
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dgn-np:NP446396.RAhz-6_kSque5rw1uPByYWzmwa-wmH3wErARiNcdXtnLc130_publicationInfo
{
this:
dcterms:created
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xsd:dateTime
;
dcterms:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dcterms:rightsHolder
dgn-void:IBIGroup
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dcterms:subject
sio:SIO_000983
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pav:authoredBy
<
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> , <
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> , <
http://orcid.org/0000-0002-9383-528X
> , <
http://orcid.org/0000-0003-0169-8159
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<
http://orcid.org/0000-0003-0169-8159
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