@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP731752.RAEwZHQVdD8mTd6J4Y9d4FxullwD0vZvbZOGq_x1SWA7U
> .
@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:NP731752.RAEwZHQVdD8mTd6J4Y9d4FxullwD0vZvbZOGq_x1SWA7U130_head
{
this:
np:hasAssertion
dgn-np:NP731752.RAEwZHQVdD8mTd6J4Y9d4FxullwD0vZvbZOGq_x1SWA7U130_assertion
;
np:hasProvenance
dgn-np:NP731752.RAEwZHQVdD8mTd6J4Y9d4FxullwD0vZvbZOGq_x1SWA7U130_provenance
;
np:hasPublicationInfo
dgn-np:NP731752.RAEwZHQVdD8mTd6J4Y9d4FxullwD0vZvbZOGq_x1SWA7U130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP731752.RAEwZHQVdD8mTd6J4Y9d4FxullwD0vZvbZOGq_x1SWA7U130_assertion
a
np:Assertion
.
dgn-np:NP731752.RAEwZHQVdD8mTd6J4Y9d4FxullwD0vZvbZOGq_x1SWA7U130_provenance
a
np:Provenance
.
dgn-np:NP731752.RAEwZHQVdD8mTd6J4Y9d4FxullwD0vZvbZOGq_x1SWA7U130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP731752.RAEwZHQVdD8mTd6J4Y9d4FxullwD0vZvbZOGq_x1SWA7U130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0265385
a
ncit:C7057
.
dgn-gda:DGNf99eb767d2417dad741ed18a1d673ac8
sio:SIO_000628
miriam-gene:4221
,
lld:C0265385
;
a
sio:SIO_001121
.
}
dgn-np:NP731752.RAEwZHQVdD8mTd6J4Y9d4FxullwD0vZvbZOGq_x1SWA7U130_provenance
{
dgn-np:NP731752.RAEwZHQVdD8mTd6J4Y9d4FxullwD0vZvbZOGq_x1SWA7U130_assertion
dcterms:description
"[Multiple endocrine neoplasia type 1 (MEN1) is an autosomal dominant hereditary disorder associated with mutations of the MEN1 gene and characterized by the combined occurrence of tumours of the parathyroid glands, the pancreatic islet cells and the anterior pituitary.]. 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:18549467
;
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:NP731752.RAEwZHQVdD8mTd6J4Y9d4FxullwD0vZvbZOGq_x1SWA7U130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:24+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" .
}