@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP700048.RAgf29eGWJThY1hXZzXmnz4QdwJH_hY2mVlT9KpX0Z3N8
> .
@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:NP700048.RAgf29eGWJThY1hXZzXmnz4QdwJH_hY2mVlT9KpX0Z3N8130_head
{
this:
np:hasAssertion
dgn-np:NP700048.RAgf29eGWJThY1hXZzXmnz4QdwJH_hY2mVlT9KpX0Z3N8130_assertion
;
np:hasProvenance
dgn-np:NP700048.RAgf29eGWJThY1hXZzXmnz4QdwJH_hY2mVlT9KpX0Z3N8130_provenance
;
np:hasPublicationInfo
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;
a
np:Nanopublication
.
dgn-np:NP700048.RAgf29eGWJThY1hXZzXmnz4QdwJH_hY2mVlT9KpX0Z3N8130_assertion
a
np:Assertion
.
dgn-np:NP700048.RAgf29eGWJThY1hXZzXmnz4QdwJH_hY2mVlT9KpX0Z3N8130_provenance
a
np:Provenance
.
dgn-np:NP700048.RAgf29eGWJThY1hXZzXmnz4QdwJH_hY2mVlT9KpX0Z3N8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP700048.RAgf29eGWJThY1hXZzXmnz4QdwJH_hY2mVlT9KpX0Z3N8130_assertion
{
miriam-gene:10993
a
ncit:C16612
.
lld:C0271563
a
ncit:C7057
.
dgn-gda:DGN9b92eb207f448b1a44636937a0b41079
sio:SIO_000628
miriam-gene:10993
,
lld:C0271563
;
a
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.
}
dgn-np:NP700048.RAgf29eGWJThY1hXZzXmnz4QdwJH_hY2mVlT9KpX0Z3N8130_provenance
{
dgn-np:NP700048.RAgf29eGWJThY1hXZzXmnz4QdwJH_hY2mVlT9KpX0Z3N8130_assertion
dcterms:description
"[We describe two male siblings with IGHD due to a homozygous missense GHRHR mutation who, because they were started on hGH therapy at different ages, presented with different height SDS at the onset of puberty and therefore had different predicted target heights.]. 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:15237716
;
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:NP700048.RAgf29eGWJThY1hXZzXmnz4QdwJH_hY2mVlT9KpX0Z3N8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:05+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
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dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}