@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP384846.RAKRupBBLY96Z8DhpZTYAZc8LsWMAYz4eIu0MxkPi_Bhg
> .
@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:NP384846.RAKRupBBLY96Z8DhpZTYAZc8LsWMAYz4eIu0MxkPi_Bhg130_head
{
this:
np:hasAssertion
dgn-np:NP384846.RAKRupBBLY96Z8DhpZTYAZc8LsWMAYz4eIu0MxkPi_Bhg130_assertion
;
np:hasProvenance
dgn-np:NP384846.RAKRupBBLY96Z8DhpZTYAZc8LsWMAYz4eIu0MxkPi_Bhg130_provenance
;
np:hasPublicationInfo
dgn-np:NP384846.RAKRupBBLY96Z8DhpZTYAZc8LsWMAYz4eIu0MxkPi_Bhg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP384846.RAKRupBBLY96Z8DhpZTYAZc8LsWMAYz4eIu0MxkPi_Bhg130_assertion
a
np:Assertion
.
dgn-np:NP384846.RAKRupBBLY96Z8DhpZTYAZc8LsWMAYz4eIu0MxkPi_Bhg130_provenance
a
np:Provenance
.
dgn-np:NP384846.RAKRupBBLY96Z8DhpZTYAZc8LsWMAYz4eIu0MxkPi_Bhg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP384846.RAKRupBBLY96Z8DhpZTYAZc8LsWMAYz4eIu0MxkPi_Bhg130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0027662
a
ncit:C7057
.
dgn-gda:DGN63abece03c098de0a605a0be1d302f76
sio:SIO_000628
miriam-gene:5979
,
lld:C0027662
;
a
sio:SIO_001121
.
}
dgn-np:NP384846.RAKRupBBLY96Z8DhpZTYAZc8LsWMAYz4eIu0MxkPi_Bhg130_provenance
{
dgn-np:NP384846.RAKRupBBLY96Z8DhpZTYAZc8LsWMAYz4eIu0MxkPi_Bhg130_assertion
dcterms:description
"[Different RET oncogene mutations have been found to be associated with inherited medullary thyroid carcinoma (MTC) in the context of three different syndromes including multiple endocrine neoplasia types 2A (MEN 2A) and 2B (MEN 2B) and familial medullary thyroid carcinoma (FMTC).]. 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:12604374
;
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 .
}
dgn-np:NP384846.RAKRupBBLY96Z8DhpZTYAZc8LsWMAYz4eIu0MxkPi_Bhg130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:39+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" .
}