@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP251238.RAhWUTz28wrF6RgfmwHrjgLJ_Arj2SDJBugX6ZuuJhKZE
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP251238.RAhWUTz28wrF6RgfmwHrjgLJ_Arj2SDJBugX6ZuuJhKZE130_assertion
;
np:hasProvenance
dgn-np:NP251238.RAhWUTz28wrF6RgfmwHrjgLJ_Arj2SDJBugX6ZuuJhKZE130_provenance
;
np:hasPublicationInfo
dgn-np:NP251238.RAhWUTz28wrF6RgfmwHrjgLJ_Arj2SDJBugX6ZuuJhKZE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP251238.RAhWUTz28wrF6RgfmwHrjgLJ_Arj2SDJBugX6ZuuJhKZE130_assertion
a
np:Assertion
.
dgn-np:NP251238.RAhWUTz28wrF6RgfmwHrjgLJ_Arj2SDJBugX6ZuuJhKZE130_provenance
a
np:Provenance
.
dgn-np:NP251238.RAhWUTz28wrF6RgfmwHrjgLJ_Arj2SDJBugX6ZuuJhKZE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP251238.RAhWUTz28wrF6RgfmwHrjgLJ_Arj2SDJBugX6ZuuJhKZE130_assertion
{
miriam-gene:4221
a
ncit:C16612
.
lld:C0020502
a
ncit:C7057
.
dgn-gda:DGNa1b995af0c9f97eea98c6faf70179078
sio:SIO_000628
miriam-gene:4221
,
lld:C0020502
;
a
sio:SIO_001121
.
}
dgn-np:NP251238.RAhWUTz28wrF6RgfmwHrjgLJ_Arj2SDJBugX6ZuuJhKZE130_provenance
{
dgn-np:NP251238.RAhWUTz28wrF6RgfmwHrjgLJ_Arj2SDJBugX6ZuuJhKZE130_assertion
dcterms:description
"[In addition, genome-wide patterns of somatic DNA alterations, including disparate roles for MEN1 gene inactivation, indicate that markedly different molecular pathogenetic processes exist for clonal outgrowth in severe uremic hyperparathyroidism versus common parathyroid adenomas.]. 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:12039978
;
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:NP251238.RAhWUTz28wrF6RgfmwHrjgLJ_Arj2SDJBugX6ZuuJhKZE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:20+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" .
}