@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1329158.RALNME_pVzp0wuAArxw-HW6k8_ZrHaZwuAUdzcJtZZLEY
> .
@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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{
this:
np:hasAssertion
dgn-np:NP1329158.RALNME_pVzp0wuAArxw-HW6k8_ZrHaZwuAUdzcJtZZLEY130_assertion
;
np:hasProvenance
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np:hasPublicationInfo
dgn-np:NP1329158.RALNME_pVzp0wuAArxw-HW6k8_ZrHaZwuAUdzcJtZZLEY130_publicationInfo
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a
np:Nanopublication
.
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a
np:Assertion
.
dgn-np:NP1329158.RALNME_pVzp0wuAArxw-HW6k8_ZrHaZwuAUdzcJtZZLEY130_provenance
a
np:Provenance
.
dgn-np:NP1329158.RALNME_pVzp0wuAArxw-HW6k8_ZrHaZwuAUdzcJtZZLEY130_publicationInfo
a
np:PublicationInfo
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{
miriam-gene:5979
a
ncit:C16612
.
lld:C1833921
a
ncit:C7057
.
dgn-gda:DGN934b10dd8897fbfb3021c25072e902b3
sio:SIO_000628
miriam-gene:5979
,
lld:C1833921
;
a
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.
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dgn-np:NP1329158.RALNME_pVzp0wuAArxw-HW6k8_ZrHaZwuAUdzcJtZZLEY130_provenance
{
dgn-np:NP1329158.RALNME_pVzp0wuAArxw-HW6k8_ZrHaZwuAUdzcJtZZLEY130_assertion
dcterms:description
"[Since germline mutations in the RET proto-oncogene (RET) predisposing to tumor development in Familial Medullary Thyroid Carcinoma (FMTC), Multiple endocrine neoplasia type 2A (MEN 2A), and Multiple endocrine neoplasia type 2B (MEN 2B) were reported, it has become possible to identify gene carriers with a very high degree of accuracy.]. 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:7987299
;
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 .
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dgn-np:NP1329158.RALNME_pVzp0wuAArxw-HW6k8_ZrHaZwuAUdzcJtZZLEY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:48+02:00"^^
xsd:dateTime
;
dcterms:rights
<
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> ;
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
> , <
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> ;
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<
http://orcid.org/0000-0003-0169-8159
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