@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP178878.RAOtGNQQ_Q_ZGaplb-6OfU7NSpK4Ql5yA-BHOvQDJqWSY
> .
@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/
> .
dgn-np:NP178878.RAOtGNQQ_Q_ZGaplb-6OfU7NSpK4Ql5yA-BHOvQDJqWSY130_head
{
this:
np:hasAssertion
dgn-np:NP178878.RAOtGNQQ_Q_ZGaplb-6OfU7NSpK4Ql5yA-BHOvQDJqWSY130_assertion
;
np:hasProvenance
dgn-np:NP178878.RAOtGNQQ_Q_ZGaplb-6OfU7NSpK4Ql5yA-BHOvQDJqWSY130_provenance
;
np:hasPublicationInfo
dgn-np:NP178878.RAOtGNQQ_Q_ZGaplb-6OfU7NSpK4Ql5yA-BHOvQDJqWSY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP178878.RAOtGNQQ_Q_ZGaplb-6OfU7NSpK4Ql5yA-BHOvQDJqWSY130_assertion
a
np:Assertion
.
dgn-np:NP178878.RAOtGNQQ_Q_ZGaplb-6OfU7NSpK4Ql5yA-BHOvQDJqWSY130_provenance
a
np:Provenance
.
dgn-np:NP178878.RAOtGNQQ_Q_ZGaplb-6OfU7NSpK4Ql5yA-BHOvQDJqWSY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP178878.RAOtGNQQ_Q_ZGaplb-6OfU7NSpK4Ql5yA-BHOvQDJqWSY130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0206693
a
ncit:C7057
.
dgn-gda:DGN1e499fa47e976bd54cb76659b9b3918b
sio:SIO_000628
miriam-gene:5979
,
lld:C0206693
;
a
sio:SIO_001122
.
}
dgn-np:NP178878.RAOtGNQQ_Q_ZGaplb-6OfU7NSpK4Ql5yA-BHOvQDJqWSY130_provenance
{
dgn-np:NP178878.RAOtGNQQ_Q_ZGaplb-6OfU7NSpK4Ql5yA-BHOvQDJqWSY130_assertion
dcterms:description
"[This intracellular mutation can initiate the full spectrum of MEN2a, initiates MTC at an early age, and causes recurrence and death if undertreated. We recommend stringent adherence to established guidance in MEN2a in this rare mutation.]. 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:20554711
;
prov:wasDerivedFrom
dgn-void:gad-20150221
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20150221
pav:importedOn
"2015-02-21"^^
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:NP178878.RAOtGNQQ_Q_ZGaplb-6OfU7NSpK4Ql5yA-BHOvQDJqWSY130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:08+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}