@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP938237.RAYDZPK2L3rf4hRNJFLIGGDBn7U2uIVOHNomvago3PS2I
> .
@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:NP938237.RAYDZPK2L3rf4hRNJFLIGGDBn7U2uIVOHNomvago3PS2I130_head
{
this:
np:hasAssertion
dgn-np:NP938237.RAYDZPK2L3rf4hRNJFLIGGDBn7U2uIVOHNomvago3PS2I130_assertion
;
np:hasProvenance
dgn-np:NP938237.RAYDZPK2L3rf4hRNJFLIGGDBn7U2uIVOHNomvago3PS2I130_provenance
;
np:hasPublicationInfo
dgn-np:NP938237.RAYDZPK2L3rf4hRNJFLIGGDBn7U2uIVOHNomvago3PS2I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP938237.RAYDZPK2L3rf4hRNJFLIGGDBn7U2uIVOHNomvago3PS2I130_assertion
a
np:Assertion
.
dgn-np:NP938237.RAYDZPK2L3rf4hRNJFLIGGDBn7U2uIVOHNomvago3PS2I130_provenance
a
np:Provenance
.
dgn-np:NP938237.RAYDZPK2L3rf4hRNJFLIGGDBn7U2uIVOHNomvago3PS2I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP938237.RAYDZPK2L3rf4hRNJFLIGGDBn7U2uIVOHNomvago3PS2I130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN9173282da8adc7cb01dd3ad80b8d5396
sio:SIO_000628
miriam-gene:4221
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP938237.RAYDZPK2L3rf4hRNJFLIGGDBn7U2uIVOHNomvago3PS2I130_provenance
{
dgn-np:NP938237.RAYDZPK2L3rf4hRNJFLIGGDBn7U2uIVOHNomvago3PS2I130_assertion
dcterms:description
"[The recent findings of the interaction between menin, encoded by the MEN1 gene, and the oestrogen receptor, as well as the observation of rare cases of mammary carcinomas in our heterozygous Men1 mutant mice, led us to investigate a putative tumour suppressor function of the Men1 gene in mouse mammary cells by disrupting the gene in luminal epithelial cells.]. 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:23180448
;
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:NP938237.RAYDZPK2L3rf4hRNJFLIGGDBn7U2uIVOHNomvago3PS2I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:35+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
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}