@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP564087.RAOe5oUF7dJCZ-A7cPgOM5Q1s7IVArrZCO-B-D3memqyA
> .
@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:NP564087.RAOe5oUF7dJCZ-A7cPgOM5Q1s7IVArrZCO-B-D3memqyA130_head
{
this:
np:hasAssertion
dgn-np:NP564087.RAOe5oUF7dJCZ-A7cPgOM5Q1s7IVArrZCO-B-D3memqyA130_assertion
;
np:hasProvenance
dgn-np:NP564087.RAOe5oUF7dJCZ-A7cPgOM5Q1s7IVArrZCO-B-D3memqyA130_provenance
;
np:hasPublicationInfo
dgn-np:NP564087.RAOe5oUF7dJCZ-A7cPgOM5Q1s7IVArrZCO-B-D3memqyA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP564087.RAOe5oUF7dJCZ-A7cPgOM5Q1s7IVArrZCO-B-D3memqyA130_assertion
a
np:Assertion
.
dgn-np:NP564087.RAOe5oUF7dJCZ-A7cPgOM5Q1s7IVArrZCO-B-D3memqyA130_provenance
a
np:Provenance
.
dgn-np:NP564087.RAOe5oUF7dJCZ-A7cPgOM5Q1s7IVArrZCO-B-D3memqyA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP564087.RAOe5oUF7dJCZ-A7cPgOM5Q1s7IVArrZCO-B-D3memqyA130_assertion
{
miriam-gene:2688
a
ncit:C16612
.
lld:C0497552
a
ncit:C7057
.
dgn-gda:DGN861c57b880563b46bfc5a29fb3bdae82
sio:SIO_000628
miriam-gene:2688
,
lld:C0497552
;
a
sio:SIO_001121
.
}
dgn-np:NP564087.RAOe5oUF7dJCZ-A7cPgOM5Q1s7IVArrZCO-B-D3memqyA130_provenance
{
dgn-np:NP564087.RAOe5oUF7dJCZ-A7cPgOM5Q1s7IVArrZCO-B-D3memqyA130_assertion
dcterms:description
"[When a child is not following the normal, predicted growth curve, an evaluation for underlying illness and central nervous system abnormalities is required and appropriate consideration should be given to genetic defects causing growth hormone (GH) deficiency.]. 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:17336732
;
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:NP564087.RAOe5oUF7dJCZ-A7cPgOM5Q1s7IVArrZCO-B-D3memqyA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}