@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1324242.RAEVtRB3W2f39giQdruNR2JExNrcLpIuIY0AnDjtuWjFc
> .
@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:NP1324242.RAEVtRB3W2f39giQdruNR2JExNrcLpIuIY0AnDjtuWjFc130_head
{
this:
np:hasAssertion
dgn-np:NP1324242.RAEVtRB3W2f39giQdruNR2JExNrcLpIuIY0AnDjtuWjFc130_assertion
;
np:hasProvenance
dgn-np:NP1324242.RAEVtRB3W2f39giQdruNR2JExNrcLpIuIY0AnDjtuWjFc130_provenance
;
np:hasPublicationInfo
dgn-np:NP1324242.RAEVtRB3W2f39giQdruNR2JExNrcLpIuIY0AnDjtuWjFc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1324242.RAEVtRB3W2f39giQdruNR2JExNrcLpIuIY0AnDjtuWjFc130_assertion
a
np:Assertion
.
dgn-np:NP1324242.RAEVtRB3W2f39giQdruNR2JExNrcLpIuIY0AnDjtuWjFc130_provenance
a
np:Provenance
.
dgn-np:NP1324242.RAEVtRB3W2f39giQdruNR2JExNrcLpIuIY0AnDjtuWjFc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1324242.RAEVtRB3W2f39giQdruNR2JExNrcLpIuIY0AnDjtuWjFc130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0025268
a
ncit:C7057
.
dgn-gda:DGN56bfb00821e6ba444215d254a7cfc35e
sio:SIO_000628
miriam-gene:5979
,
lld:C0025268
;
a
sio:SIO_001121
.
}
dgn-np:NP1324242.RAEVtRB3W2f39giQdruNR2JExNrcLpIuIY0AnDjtuWjFc130_provenance
{
dgn-np:NP1324242.RAEVtRB3W2f39giQdruNR2JExNrcLpIuIY0AnDjtuWjFc130_assertion
dcterms:description
"[Recently specific point mutations of RET have been demonstrated to be responsible for the Multiple Endocrine Neoplasia type 2A and 2B and Familial Medullary Thyroid Carcinoma syndromes, characterized by the occurrence of medullary thyroid carcinomas.]. 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:7864888
;
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:NP1324242.RAEVtRB3W2f39giQdruNR2JExNrcLpIuIY0AnDjtuWjFc130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:46+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" .
}