@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP462142.RA2iE0Kkh7PPXH1tVqtjld1foG5IctInDrRQq8mxofEqQ
> .
@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:NP462142.RA2iE0Kkh7PPXH1tVqtjld1foG5IctInDrRQq8mxofEqQ130_head
{
this:
np:hasAssertion
dgn-np:NP462142.RA2iE0Kkh7PPXH1tVqtjld1foG5IctInDrRQq8mxofEqQ130_assertion
;
np:hasProvenance
dgn-np:NP462142.RA2iE0Kkh7PPXH1tVqtjld1foG5IctInDrRQq8mxofEqQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP462142.RA2iE0Kkh7PPXH1tVqtjld1foG5IctInDrRQq8mxofEqQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP462142.RA2iE0Kkh7PPXH1tVqtjld1foG5IctInDrRQq8mxofEqQ130_assertion
a
np:Assertion
.
dgn-np:NP462142.RA2iE0Kkh7PPXH1tVqtjld1foG5IctInDrRQq8mxofEqQ130_provenance
a
np:Provenance
.
dgn-np:NP462142.RA2iE0Kkh7PPXH1tVqtjld1foG5IctInDrRQq8mxofEqQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP462142.RA2iE0Kkh7PPXH1tVqtjld1foG5IctInDrRQq8mxofEqQ130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0014132
a
ncit:C7057
.
dgn-gda:DGNa1871b8e1b1fb65321402e69f1a86efe
sio:SIO_000628
miriam-gene:4221
,
lld:C0014132
;
a
sio:SIO_001121
.
}
dgn-np:NP462142.RA2iE0Kkh7PPXH1tVqtjld1foG5IctInDrRQq8mxofEqQ130_provenance
{
dgn-np:NP462142.RA2iE0Kkh7PPXH1tVqtjld1foG5IctInDrRQq8mxofEqQ130_assertion
dcterms:description
"[In addition, we discuss not only how the Men1 mutants have shed light on the role of menin in endocrine tumor suppression, but also how Men1 mutant mice have helped uncover previously unrecognized roles for menin in development, leukemogenesis and gestational diabetes.]. 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:20175458
;
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:NP462142.RA2iE0Kkh7PPXH1tVqtjld1foG5IctInDrRQq8mxofEqQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:35+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
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pav:version
"v2.1.0" .
}