@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP553573.RAj3E2OWuxOsL33kkn7GHhuEvNzJSaeyHdD03UR4Eo5oE
> .
@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/v3.0.0/void/
> .
dgn-np:NP553573.RAj3E2OWuxOsL33kkn7GHhuEvNzJSaeyHdD03UR4Eo5oE130_head
{
this:
np:hasAssertion
dgn-np:NP553573.RAj3E2OWuxOsL33kkn7GHhuEvNzJSaeyHdD03UR4Eo5oE130_assertion
;
np:hasProvenance
dgn-np:NP553573.RAj3E2OWuxOsL33kkn7GHhuEvNzJSaeyHdD03UR4Eo5oE130_provenance
;
np:hasPublicationInfo
dgn-np:NP553573.RAj3E2OWuxOsL33kkn7GHhuEvNzJSaeyHdD03UR4Eo5oE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP553573.RAj3E2OWuxOsL33kkn7GHhuEvNzJSaeyHdD03UR4Eo5oE130_assertion
a
np:Assertion
.
dgn-np:NP553573.RAj3E2OWuxOsL33kkn7GHhuEvNzJSaeyHdD03UR4Eo5oE130_provenance
a
np:Provenance
.
dgn-np:NP553573.RAj3E2OWuxOsL33kkn7GHhuEvNzJSaeyHdD03UR4Eo5oE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP553573.RAj3E2OWuxOsL33kkn7GHhuEvNzJSaeyHdD03UR4Eo5oE130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0346306
a
ncit:C7057
.
dgn-gda:DGN5e4347922a36f5178d307bd3ee9daf92
sio:SIO_000628
miriam-gene:4221
,
lld:C0346306
;
a
sio:SIO_001121
.
}
dgn-np:NP553573.RAj3E2OWuxOsL33kkn7GHhuEvNzJSaeyHdD03UR4Eo5oE130_provenance
{
dgn-np:NP553573.RAj3E2OWuxOsL33kkn7GHhuEvNzJSaeyHdD03UR4Eo5oE130_assertion
dcterms:description
"[All patients with an enteropancreatic lesion were mutation carriers and the absence of mutation in three apparently sporadic MEN1 patients with only hyperparathyroidism and pituitary microadenoma might represent the presence of MEN1 phenocopy.]. 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:12807514
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP553573.RAj3E2OWuxOsL33kkn7GHhuEvNzJSaeyHdD03UR4Eo5oE130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:07+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}