@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP791017.RAsXnoOkdBLKo2CegU2bsCmUSYj3hQAnaB3Fd79jGBYcs
> .
@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:NP791017.RAsXnoOkdBLKo2CegU2bsCmUSYj3hQAnaB3Fd79jGBYcs130_head
{
this:
np:hasAssertion
dgn-np:NP791017.RAsXnoOkdBLKo2CegU2bsCmUSYj3hQAnaB3Fd79jGBYcs130_assertion
;
np:hasProvenance
dgn-np:NP791017.RAsXnoOkdBLKo2CegU2bsCmUSYj3hQAnaB3Fd79jGBYcs130_provenance
;
np:hasPublicationInfo
dgn-np:NP791017.RAsXnoOkdBLKo2CegU2bsCmUSYj3hQAnaB3Fd79jGBYcs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP791017.RAsXnoOkdBLKo2CegU2bsCmUSYj3hQAnaB3Fd79jGBYcs130_assertion
a
np:Assertion
.
dgn-np:NP791017.RAsXnoOkdBLKo2CegU2bsCmUSYj3hQAnaB3Fd79jGBYcs130_provenance
a
np:Provenance
.
dgn-np:NP791017.RAsXnoOkdBLKo2CegU2bsCmUSYj3hQAnaB3Fd79jGBYcs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP791017.RAsXnoOkdBLKo2CegU2bsCmUSYj3hQAnaB3Fd79jGBYcs130_assertion
{
miriam-gene:8091
a
ncit:C16612
.
lld:C0013336
a
ncit:C7057
.
dgn-gda:DGNe68688c5c2545903a85af04b88dafeb5
sio:SIO_000628
miriam-gene:8091
,
lld:C0013336
;
a
sio:SIO_001121
.
}
dgn-np:NP791017.RAsXnoOkdBLKo2CegU2bsCmUSYj3hQAnaB3Fd79jGBYcs130_provenance
{
dgn-np:NP791017.RAsXnoOkdBLKo2CegU2bsCmUSYj3hQAnaB3Fd79jGBYcs130_assertion
dcterms:description
"[The identification of an intragenic HMGA2 deletion in a boy with proportionate short stature and the cosegregation of this deletion with reduced adult height in the extended family of the boy further underscore the role of HMGA2 in regulating human linear growth.]. 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:19298872
;
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:NP791017.RAsXnoOkdBLKo2CegU2bsCmUSYj3hQAnaB3Fd79jGBYcs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:05+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" .
}