@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1369316.RAjGy57khoAvA-gbghv-lhY9_c3lPE47sTa1CjIYvZzc0
> .
@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:NP1369316.RAjGy57khoAvA-gbghv-lhY9_c3lPE47sTa1CjIYvZzc0130_head
{
this:
np:hasAssertion
dgn-np:NP1369316.RAjGy57khoAvA-gbghv-lhY9_c3lPE47sTa1CjIYvZzc0130_assertion
;
np:hasProvenance
dgn-np:NP1369316.RAjGy57khoAvA-gbghv-lhY9_c3lPE47sTa1CjIYvZzc0130_provenance
;
np:hasPublicationInfo
dgn-np:NP1369316.RAjGy57khoAvA-gbghv-lhY9_c3lPE47sTa1CjIYvZzc0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1369316.RAjGy57khoAvA-gbghv-lhY9_c3lPE47sTa1CjIYvZzc0130_assertion
a
np:Assertion
.
dgn-np:NP1369316.RAjGy57khoAvA-gbghv-lhY9_c3lPE47sTa1CjIYvZzc0130_provenance
a
np:Provenance
.
dgn-np:NP1369316.RAjGy57khoAvA-gbghv-lhY9_c3lPE47sTa1CjIYvZzc0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1369316.RAjGy57khoAvA-gbghv-lhY9_c3lPE47sTa1CjIYvZzc0130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0025269
a
ncit:C7057
.
dgn-gda:DGNbb30d550a7b471245c6f026d06e22698
sio:SIO_000628
miriam-gene:5979
,
lld:C0025269
;
a
sio:SIO_001121
.
}
dgn-np:NP1369316.RAjGy57khoAvA-gbghv-lhY9_c3lPE47sTa1CjIYvZzc0130_provenance
{
dgn-np:NP1369316.RAjGy57khoAvA-gbghv-lhY9_c3lPE47sTa1CjIYvZzc0130_assertion
dcterms:description
"[Germline mutations in exons 10, 11, and 16 of the RET protooncogene are associated with the heritable cancer syndromes multiple endocrine neoplasia (MEN) type 2A, familial medullary thyroid carcinoma (FMTC), and MEN type 2B.]. 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:9068588
;
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:NP1369316.RAjGy57khoAvA-gbghv-lhY9_c3lPE47sTa1CjIYvZzc0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:06+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" .
}