@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP606604.RA7QPRCkTXaPQVgPaOOs5LNucKU3v0iYgy-OOOaGRMxi4
> .
@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:NP606604.RA7QPRCkTXaPQVgPaOOs5LNucKU3v0iYgy-OOOaGRMxi4130_head
{
this:
np:hasAssertion
dgn-np:NP606604.RA7QPRCkTXaPQVgPaOOs5LNucKU3v0iYgy-OOOaGRMxi4130_assertion
;
np:hasProvenance
dgn-np:NP606604.RA7QPRCkTXaPQVgPaOOs5LNucKU3v0iYgy-OOOaGRMxi4130_provenance
;
np:hasPublicationInfo
dgn-np:NP606604.RA7QPRCkTXaPQVgPaOOs5LNucKU3v0iYgy-OOOaGRMxi4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP606604.RA7QPRCkTXaPQVgPaOOs5LNucKU3v0iYgy-OOOaGRMxi4130_assertion
a
np:Assertion
.
dgn-np:NP606604.RA7QPRCkTXaPQVgPaOOs5LNucKU3v0iYgy-OOOaGRMxi4130_provenance
a
np:Provenance
.
dgn-np:NP606604.RA7QPRCkTXaPQVgPaOOs5LNucKU3v0iYgy-OOOaGRMxi4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP606604.RA7QPRCkTXaPQVgPaOOs5LNucKU3v0iYgy-OOOaGRMxi4130_assertion
{
miriam-gene:8091
a
ncit:C16612
.
lld:C0033375
a
ncit:C7057
.
dgn-gda:DGNcfa0c56a5da073f3ed73d6079c982af3
sio:SIO_000628
miriam-gene:8091
,
lld:C0033375
;
a
sio:SIO_001121
.
}
dgn-np:NP606604.RA7QPRCkTXaPQVgPaOOs5LNucKU3v0iYgy-OOOaGRMxi4130_provenance
{
dgn-np:NP606604.RA7QPRCkTXaPQVgPaOOs5LNucKU3v0iYgy-OOOaGRMxi4130_assertion
dcterms:description
"[A role for chromosome 12 polysomy to promote structural instability of HMGA2 is confirmed, but the mechanism via trisomy is less prevalent in the frequently diploid NFPAs than in the usually hyperdiploid prolactinomas.]. 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:16322327
;
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:NP606604.RA7QPRCkTXaPQVgPaOOs5LNucKU3v0iYgy-OOOaGRMxi4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:04+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" .
}