@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP216364.RAujhRMF9Utuz1O-n4Gec8AjpxNd2vUaFibcdwZPSjdUQ
> .
@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:NP216364.RAujhRMF9Utuz1O-n4Gec8AjpxNd2vUaFibcdwZPSjdUQ130_head
{
this:
np:hasAssertion
dgn-np:NP216364.RAujhRMF9Utuz1O-n4Gec8AjpxNd2vUaFibcdwZPSjdUQ130_assertion
;
np:hasProvenance
dgn-np:NP216364.RAujhRMF9Utuz1O-n4Gec8AjpxNd2vUaFibcdwZPSjdUQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP216364.RAujhRMF9Utuz1O-n4Gec8AjpxNd2vUaFibcdwZPSjdUQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP216364.RAujhRMF9Utuz1O-n4Gec8AjpxNd2vUaFibcdwZPSjdUQ130_assertion
a
np:Assertion
.
dgn-np:NP216364.RAujhRMF9Utuz1O-n4Gec8AjpxNd2vUaFibcdwZPSjdUQ130_provenance
a
np:Provenance
.
dgn-np:NP216364.RAujhRMF9Utuz1O-n4Gec8AjpxNd2vUaFibcdwZPSjdUQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP216364.RAujhRMF9Utuz1O-n4Gec8AjpxNd2vUaFibcdwZPSjdUQ130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C1833921
a
ncit:C7057
.
dgn-gda:DGN08be6a94e3ecfbfcd75c4fbd577750b9
sio:SIO_000628
miriam-gene:5979
,
lld:C1833921
;
a
sio:SIO_001121
.
}
dgn-np:NP216364.RAujhRMF9Utuz1O-n4Gec8AjpxNd2vUaFibcdwZPSjdUQ130_provenance
{
dgn-np:NP216364.RAujhRMF9Utuz1O-n4Gec8AjpxNd2vUaFibcdwZPSjdUQ130_assertion
dcterms:description
"[Missense germline mutations of the RET proto-oncogene have recently been identified in the hereditary cancer syndromes MEN2A, MEN2B, and FMTC, all characterized by medullary carcinoma, but also including phaeochromocytoma in MEN2A and MEN2B and parathyroid disease in MEN2A.]. 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:8976870
;
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:NP216364.RAujhRMF9Utuz1O-n4Gec8AjpxNd2vUaFibcdwZPSjdUQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:00+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" .
}