@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP356916.RAgHWvCC7KAvStXYK09Ajyw_L5v91lDq2XPIrmeIA2Y4A
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP356916.RAgHWvCC7KAvStXYK09Ajyw_L5v91lDq2XPIrmeIA2Y4A130_head
{
this:
np:hasAssertion
dgn-np:NP356916.RAgHWvCC7KAvStXYK09Ajyw_L5v91lDq2XPIrmeIA2Y4A130_assertion
;
np:hasProvenance
dgn-np:NP356916.RAgHWvCC7KAvStXYK09Ajyw_L5v91lDq2XPIrmeIA2Y4A130_provenance
;
np:hasPublicationInfo
dgn-np:NP356916.RAgHWvCC7KAvStXYK09Ajyw_L5v91lDq2XPIrmeIA2Y4A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP356916.RAgHWvCC7KAvStXYK09Ajyw_L5v91lDq2XPIrmeIA2Y4A130_assertion
a
np:Assertion
.
dgn-np:NP356916.RAgHWvCC7KAvStXYK09Ajyw_L5v91lDq2XPIrmeIA2Y4A130_provenance
a
np:Provenance
.
dgn-np:NP356916.RAgHWvCC7KAvStXYK09Ajyw_L5v91lDq2XPIrmeIA2Y4A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP356916.RAgHWvCC7KAvStXYK09Ajyw_L5v91lDq2XPIrmeIA2Y4A130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0025267
a
ncit:C7057
.
dgn-gda:DGN7a4e00f9821a6e03950e11fc74e32923
sio:SIO_000628
miriam-gene:4221
,
lld:C0025267
;
a
sio:SIO_001121
.
}
dgn-np:NP356916.RAgHWvCC7KAvStXYK09Ajyw_L5v91lDq2XPIrmeIA2Y4A130_provenance
{
dgn-np:NP356916.RAgHWvCC7KAvStXYK09Ajyw_L5v91lDq2XPIrmeIA2Y4A130_assertion
dcterms:description
"[Multiple endocrine neoplasia type 1 (MEN 1) syndrome is an autosomal dominant disorder caused by germline mutations in the MEN1 gene and characterized by multiple endocrine tumors, most notably in the parathyroid glands, pituitary, and pancreas.]. 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:12049533
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP356916.RAgHWvCC7KAvStXYK09Ajyw_L5v91lDq2XPIrmeIA2Y4A130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:44:27+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}