@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP432749.RATgfIQvaW3kgGUaMEzsb09oZk38D2gOG05AsDtVU6qAg
> .
@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/eco.owl#
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/2.0/
> .
@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/nanopublications.trig#
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/gene-disease-association.ttl#
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v2.1.0/void.ttl#
> .
dgn-np:NP432749.RATgfIQvaW3kgGUaMEzsb09oZk38D2gOG05AsDtVU6qAg130_head
{
this:
np:hasAssertion
dgn-np:NP432749.RATgfIQvaW3kgGUaMEzsb09oZk38D2gOG05AsDtVU6qAg130_assertion
;
np:hasProvenance
dgn-np:NP432749.RATgfIQvaW3kgGUaMEzsb09oZk38D2gOG05AsDtVU6qAg130_provenance
;
np:hasPublicationInfo
dgn-np:NP432749.RATgfIQvaW3kgGUaMEzsb09oZk38D2gOG05AsDtVU6qAg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP432749.RATgfIQvaW3kgGUaMEzsb09oZk38D2gOG05AsDtVU6qAg130_assertion
a
np:Assertion
.
dgn-np:NP432749.RATgfIQvaW3kgGUaMEzsb09oZk38D2gOG05AsDtVU6qAg130_provenance
a
np:Provenance
.
dgn-np:NP432749.RATgfIQvaW3kgGUaMEzsb09oZk38D2gOG05AsDtVU6qAg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP432749.RATgfIQvaW3kgGUaMEzsb09oZk38D2gOG05AsDtVU6qAg130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0027672
a
ncit:C7057
.
dgn-gda:DGNbae6eed5b73d8e83d20d8779b66772c8
sio:SIO_000628
miriam-gene:5979
,
lld:C0027672
;
a
sio:SIO_001121
.
}
dgn-np:NP432749.RATgfIQvaW3kgGUaMEzsb09oZk38D2gOG05AsDtVU6qAg130_provenance
{
dgn-np:NP432749.RATgfIQvaW3kgGUaMEzsb09oZk38D2gOG05AsDtVU6qAg130_assertion
dcterms:description
"[The ret protooncogene (RET), shown to be rearranged in human papillary thyroid cancers (PTC), has been mapped by in situ hybridization to 10q11.2 near the predisposition locus for the inherited cancer syndrome multiple endocrine neoplasia type 2 (MEN 2).]. 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:7903002
;
prov:wasDerivedFrom
dgn-void:befree-20140225
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20140225
pav:importedOn
"2014-02-25"^^
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:NP432749.RATgfIQvaW3kgGUaMEzsb09oZk38D2gOG05AsDtVU6qAg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:16+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:disgenetrdf
;
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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}