@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP589330.RAgeEk9aR98gXo3DB_Iw6_ZA5id5GdY1gpMhcg179ZMk4
> .
@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:NP589330.RAgeEk9aR98gXo3DB_Iw6_ZA5id5GdY1gpMhcg179ZMk4130_head
{
this:
np:hasAssertion
dgn-np:NP589330.RAgeEk9aR98gXo3DB_Iw6_ZA5id5GdY1gpMhcg179ZMk4130_assertion
;
np:hasProvenance
dgn-np:NP589330.RAgeEk9aR98gXo3DB_Iw6_ZA5id5GdY1gpMhcg179ZMk4130_provenance
;
np:hasPublicationInfo
dgn-np:NP589330.RAgeEk9aR98gXo3DB_Iw6_ZA5id5GdY1gpMhcg179ZMk4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP589330.RAgeEk9aR98gXo3DB_Iw6_ZA5id5GdY1gpMhcg179ZMk4130_assertion
a
np:Assertion
.
dgn-np:NP589330.RAgeEk9aR98gXo3DB_Iw6_ZA5id5GdY1gpMhcg179ZMk4130_provenance
a
np:Provenance
.
dgn-np:NP589330.RAgeEk9aR98gXo3DB_Iw6_ZA5id5GdY1gpMhcg179ZMk4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP589330.RAgeEk9aR98gXo3DB_Iw6_ZA5id5GdY1gpMhcg179ZMk4130_assertion
{
miriam-gene:11151
a
ncit:C16612
.
lld:C0020459
a
ncit:C7057
.
dgn-gda:DGN4f5cb9e9d322b23c30313aa41c3498f0
sio:SIO_000628
miriam-gene:11151
,
lld:C0020459
;
a
sio:SIO_001121
.
}
dgn-np:NP589330.RAgeEk9aR98gXo3DB_Iw6_ZA5id5GdY1gpMhcg179ZMk4130_provenance
{
dgn-np:NP589330.RAgeEk9aR98gXo3DB_Iw6_ZA5id5GdY1gpMhcg179ZMk4130_assertion
dcterms:description
"[In order to evaluate whether all cases of focal hyperinsulinism are caused by this mechanism, 56 pancreatectomy specimens with focal hyperinsulinism were tested for the loss of maternal allele by two methods: immunohistochemistry for p57(kip2) (n=56) and microsatellite marker analysis (n=27).]. 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:16357843
;
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:NP589330.RAgeEk9aR98gXo3DB_Iw6_ZA5id5GdY1gpMhcg179ZMk4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:54+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" .
}