@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP451148.RAHssMn7a8q5NjVQmWTkyU10zrqs1brio3DT5elPoPq7o
> .
@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:NP451148.RAHssMn7a8q5NjVQmWTkyU10zrqs1brio3DT5elPoPq7o130_head
{
this:
np:hasAssertion
dgn-np:NP451148.RAHssMn7a8q5NjVQmWTkyU10zrqs1brio3DT5elPoPq7o130_assertion
;
np:hasProvenance
dgn-np:NP451148.RAHssMn7a8q5NjVQmWTkyU10zrqs1brio3DT5elPoPq7o130_provenance
;
np:hasPublicationInfo
dgn-np:NP451148.RAHssMn7a8q5NjVQmWTkyU10zrqs1brio3DT5elPoPq7o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP451148.RAHssMn7a8q5NjVQmWTkyU10zrqs1brio3DT5elPoPq7o130_assertion
a
np:Assertion
.
dgn-np:NP451148.RAHssMn7a8q5NjVQmWTkyU10zrqs1brio3DT5elPoPq7o130_provenance
a
np:Provenance
.
dgn-np:NP451148.RAHssMn7a8q5NjVQmWTkyU10zrqs1brio3DT5elPoPq7o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP451148.RAHssMn7a8q5NjVQmWTkyU10zrqs1brio3DT5elPoPq7o130_assertion
{
miriam-gene:1028
a
ncit:C16612
.
lld:C0206667
a
ncit:C7057
.
dgn-gda:DGNc8441d3b74cf1b7b9d4417c4a2f216ed
sio:SIO_000628
miriam-gene:1028
,
lld:C0206667
;
a
sio:SIO_001121
.
}
dgn-np:NP451148.RAHssMn7a8q5NjVQmWTkyU10zrqs1brio3DT5elPoPq7o130_provenance
{
dgn-np:NP451148.RAHssMn7a8q5NjVQmWTkyU10zrqs1brio3DT5elPoPq7o130_assertion
dcterms:description
"[p57KIP2 mRNA (and H19 RNA) was abundantly expressed in normal human adrenals, adrenocortical adenomas from patients with Cushing's or Conn's syndrome or without clinical evidence of hormone overproduction, hyperplastic adrenals, and tumor-adjacent adrenal tissues, in which IGF-II mRNA expression was low.]. 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:9177379
;
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:NP451148.RAHssMn7a8q5NjVQmWTkyU10zrqs1brio3DT5elPoPq7o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:29+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" .
}