@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP828553.RAvDvkdkiM08g3YOorxYONEKiganGWR45GkzPao36d-VQ
> .
@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:NP828553.RAvDvkdkiM08g3YOorxYONEKiganGWR45GkzPao36d-VQ130_head
{
this:
np:hasAssertion
dgn-np:NP828553.RAvDvkdkiM08g3YOorxYONEKiganGWR45GkzPao36d-VQ130_assertion
;
np:hasProvenance
dgn-np:NP828553.RAvDvkdkiM08g3YOorxYONEKiganGWR45GkzPao36d-VQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP828553.RAvDvkdkiM08g3YOorxYONEKiganGWR45GkzPao36d-VQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP828553.RAvDvkdkiM08g3YOorxYONEKiganGWR45GkzPao36d-VQ130_assertion
a
np:Assertion
.
dgn-np:NP828553.RAvDvkdkiM08g3YOorxYONEKiganGWR45GkzPao36d-VQ130_provenance
a
np:Provenance
.
dgn-np:NP828553.RAvDvkdkiM08g3YOorxYONEKiganGWR45GkzPao36d-VQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP828553.RAvDvkdkiM08g3YOorxYONEKiganGWR45GkzPao36d-VQ130_assertion
{
miriam-gene:3952
a
ncit:C16612
.
lld:C1845118
a
ncit:C7057
.
dgn-gda:DGNd8357e1f14a6ddfc1d5924af266f48f2
sio:SIO_000628
miriam-gene:3952
,
lld:C1845118
;
a
sio:SIO_001121
.
}
dgn-np:NP828553.RAvDvkdkiM08g3YOorxYONEKiganGWR45GkzPao36d-VQ130_provenance
{
dgn-np:NP828553.RAvDvkdkiM08g3YOorxYONEKiganGWR45GkzPao36d-VQ130_assertion
dcterms:description
"[We hypothesized that responses to growth hormone (GH) therapy by idiopathic short stature (ISS) and growth hormone deficiency (GHD) patients were associated with single nucleotide polymorphisms (SNPs) in the leptin (LEP) and leptin receptor (LEPR) genes.]. 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:23009903
;
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:NP828553.RAvDvkdkiM08g3YOorxYONEKiganGWR45GkzPao36d-VQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:27+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" .
}