@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP177063.RA3rxe0uxxB915Ov1DPLSTY3-bT2z51hs1tfy8RZXWFik
> .
@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:NP177063.RA3rxe0uxxB915Ov1DPLSTY3-bT2z51hs1tfy8RZXWFik130_head
{
this:
np:hasAssertion
dgn-np:NP177063.RA3rxe0uxxB915Ov1DPLSTY3-bT2z51hs1tfy8RZXWFik130_assertion
;
np:hasProvenance
dgn-np:NP177063.RA3rxe0uxxB915Ov1DPLSTY3-bT2z51hs1tfy8RZXWFik130_provenance
;
np:hasPublicationInfo
dgn-np:NP177063.RA3rxe0uxxB915Ov1DPLSTY3-bT2z51hs1tfy8RZXWFik130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP177063.RA3rxe0uxxB915Ov1DPLSTY3-bT2z51hs1tfy8RZXWFik130_assertion
a
np:Assertion
.
dgn-np:NP177063.RA3rxe0uxxB915Ov1DPLSTY3-bT2z51hs1tfy8RZXWFik130_provenance
a
np:Provenance
.
dgn-np:NP177063.RA3rxe0uxxB915Ov1DPLSTY3-bT2z51hs1tfy8RZXWFik130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP177063.RA3rxe0uxxB915Ov1DPLSTY3-bT2z51hs1tfy8RZXWFik130_assertion
{
miriam-gene:2688
a
ncit:C16612
.
lld:C0271561
a
ncit:C7057
.
dgn-gda:DGN03c31a8fd27d280ca2966a7554d20698
sio:SIO_000628
miriam-gene:2688
,
lld:C0271561
;
a
sio:SIO_001121
.
}
dgn-np:NP177063.RA3rxe0uxxB915Ov1DPLSTY3-bT2z51hs1tfy8RZXWFik130_provenance
{
dgn-np:NP177063.RA3rxe0uxxB915Ov1DPLSTY3-bT2z51hs1tfy8RZXWFik130_assertion
dcterms:description
"[One strategy for optimizing growth hormone (GH) treatment is to develop mathematical models based on clinical data from the large numbers of subjects in the KIGS (Pfizer International Growth Study Database) and to compare the observed versus predicted growth responses in subjects with short stature secondary to idiopathic GH deficiency (GHD), Turner syndrome, small birth size and idiopathic causes of short stature.]. 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:18174708
;
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:NP177063.RA3rxe0uxxB915Ov1DPLSTY3-bT2z51hs1tfy8RZXWFik130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:35+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" .
}