@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP592008.RAQf9CusIGmwYyF5l6KUVGMPoJTUj9m7F6wK1plT1Y5S8
> .
@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:NP592008.RAQf9CusIGmwYyF5l6KUVGMPoJTUj9m7F6wK1plT1Y5S8130_head
{
this:
np:hasAssertion
dgn-np:NP592008.RAQf9CusIGmwYyF5l6KUVGMPoJTUj9m7F6wK1plT1Y5S8130_assertion
;
np:hasProvenance
dgn-np:NP592008.RAQf9CusIGmwYyF5l6KUVGMPoJTUj9m7F6wK1plT1Y5S8130_provenance
;
np:hasPublicationInfo
dgn-np:NP592008.RAQf9CusIGmwYyF5l6KUVGMPoJTUj9m7F6wK1plT1Y5S8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP592008.RAQf9CusIGmwYyF5l6KUVGMPoJTUj9m7F6wK1plT1Y5S8130_assertion
a
np:Assertion
.
dgn-np:NP592008.RAQf9CusIGmwYyF5l6KUVGMPoJTUj9m7F6wK1plT1Y5S8130_provenance
a
np:Provenance
.
dgn-np:NP592008.RAQf9CusIGmwYyF5l6KUVGMPoJTUj9m7F6wK1plT1Y5S8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP592008.RAQf9CusIGmwYyF5l6KUVGMPoJTUj9m7F6wK1plT1Y5S8130_assertion
{
miriam-gene:3479
a
ncit:C16612
.
lld:C1845118
a
ncit:C7057
.
dgn-gda:DGN2663592d25d536002768d9625f99c64c
sio:SIO_000628
miriam-gene:3479
,
lld:C1845118
;
a
sio:SIO_001121
.
}
dgn-np:NP592008.RAQf9CusIGmwYyF5l6KUVGMPoJTUj9m7F6wK1plT1Y5S8130_provenance
{
dgn-np:NP592008.RAQf9CusIGmwYyF5l6KUVGMPoJTUj9m7F6wK1plT1Y5S8130_assertion
dcterms:description
"[Low levels of GH binding protein may indicate mutations in the extracellular domain of the receptor, and by focusing on 14 children with ISS who had low GH binding protein and insulin-like growth factor I levels, we found three heterozygotes and one compound heterozygote for mutations in the extracellular domain of the receptor.]. 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:9255229
;
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:NP592008.RAQf9CusIGmwYyF5l6KUVGMPoJTUj9m7F6wK1plT1Y5S8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:56+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" .
}