@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY
> .
@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:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_head
{
this:
np:hasAssertion
dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_assertion
;
np:hasProvenance
dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_provenance
;
np:hasPublicationInfo
dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_assertion
a
np:Assertion
.
dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_provenance
a
np:Provenance
.
dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_assertion
{
miriam-gene:1027
a
ncit:C16612
.
lld:C0027662
a
ncit:C7057
.
dgn-gda:DGNdc83bd262570b540682174de9add10f1
sio:SIO_000628
miriam-gene:1027
,
lld:C0027662
;
a
sio:SIO_001121
.
}
dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_provenance
{
dgn-np:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_assertion
dcterms:description
"[have reported that germline mutations in CDKN1B can predispose to the development of multiple endocrine tumours in both rats and humans and this new MEN syndrome is named MENX and MEN4, respectively.]. 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:23140918
;
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:NP460215.RAPYSuyOaeg8oQxSFCIddzLPCsJYtH4yFo-S5lan8tKJY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:34+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" .
}