@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP383297.RA1SSJnVICmg79gtna3LTDG1S4mYsbX-oVvm8xPm1KT34
> .
@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:NP383297.RA1SSJnVICmg79gtna3LTDG1S4mYsbX-oVvm8xPm1KT34130_head
{
this:
np:hasAssertion
dgn-np:NP383297.RA1SSJnVICmg79gtna3LTDG1S4mYsbX-oVvm8xPm1KT34130_assertion
;
np:hasProvenance
dgn-np:NP383297.RA1SSJnVICmg79gtna3LTDG1S4mYsbX-oVvm8xPm1KT34130_provenance
;
np:hasPublicationInfo
dgn-np:NP383297.RA1SSJnVICmg79gtna3LTDG1S4mYsbX-oVvm8xPm1KT34130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP383297.RA1SSJnVICmg79gtna3LTDG1S4mYsbX-oVvm8xPm1KT34130_assertion
a
np:Assertion
.
dgn-np:NP383297.RA1SSJnVICmg79gtna3LTDG1S4mYsbX-oVvm8xPm1KT34130_provenance
a
np:Provenance
.
dgn-np:NP383297.RA1SSJnVICmg79gtna3LTDG1S4mYsbX-oVvm8xPm1KT34130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP383297.RA1SSJnVICmg79gtna3LTDG1S4mYsbX-oVvm8xPm1KT34130_assertion
{
miriam-gene:2690
a
ncit:C16612
.
lld:C0041408
a
ncit:C7057
.
dgn-gda:DGNcb60bf463822728bd93829af40478ede
sio:SIO_000628
miriam-gene:2690
,
lld:C0041408
;
a
sio:SIO_001121
.
}
dgn-np:NP383297.RA1SSJnVICmg79gtna3LTDG1S4mYsbX-oVvm8xPm1KT34130_provenance
{
dgn-np:NP383297.RA1SSJnVICmg79gtna3LTDG1S4mYsbX-oVvm8xPm1KT34130_assertion
dcterms:description
"[Studies that evaluated response to GH treatment determined by these two GHR isoforms in children with GH deficiency, girls with Turner syndrome, children born small for gestational age and patients with acromegaly showed that patients carrying the GHRd3 allele demonstrated a greater GH sensitivity than patients homozygous for the GHRfl allele.]. 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:19407498
;
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:NP383297.RA1SSJnVICmg79gtna3LTDG1S4mYsbX-oVvm8xPm1KT34130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:48+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" .
}