@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP862630.RA_gCYbQbs8Kw6R4Q_eqnuKtHfrTXh-rbtrT1QvIfbM1g
> .
@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:NP862630.RA_gCYbQbs8Kw6R4Q_eqnuKtHfrTXh-rbtrT1QvIfbM1g130_head
{
this:
np:hasAssertion
dgn-np:NP862630.RA_gCYbQbs8Kw6R4Q_eqnuKtHfrTXh-rbtrT1QvIfbM1g130_assertion
;
np:hasProvenance
dgn-np:NP862630.RA_gCYbQbs8Kw6R4Q_eqnuKtHfrTXh-rbtrT1QvIfbM1g130_provenance
;
np:hasPublicationInfo
dgn-np:NP862630.RA_gCYbQbs8Kw6R4Q_eqnuKtHfrTXh-rbtrT1QvIfbM1g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP862630.RA_gCYbQbs8Kw6R4Q_eqnuKtHfrTXh-rbtrT1QvIfbM1g130_assertion
a
np:Assertion
.
dgn-np:NP862630.RA_gCYbQbs8Kw6R4Q_eqnuKtHfrTXh-rbtrT1QvIfbM1g130_provenance
a
np:Provenance
.
dgn-np:NP862630.RA_gCYbQbs8Kw6R4Q_eqnuKtHfrTXh-rbtrT1QvIfbM1g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP862630.RA_gCYbQbs8Kw6R4Q_eqnuKtHfrTXh-rbtrT1QvIfbM1g130_assertion
{
miriam-gene:2690
a
ncit:C16612
.
lld:C0028754
a
ncit:C7057
.
dgn-gda:DGNc859617280222dd244580f8b662fd1dd
sio:SIO_000628
miriam-gene:2690
,
lld:C0028754
;
a
sio:SIO_001121
.
}
dgn-np:NP862630.RA_gCYbQbs8Kw6R4Q_eqnuKtHfrTXh-rbtrT1QvIfbM1g130_provenance
{
dgn-np:NP862630.RA_gCYbQbs8Kw6R4Q_eqnuKtHfrTXh-rbtrT1QvIfbM1g130_assertion
dcterms:description
"[In man, evaluation of the 2 largest cohorts of patients with Laron syndrome (inactive GH receptor resulting in IGF1 deficiency) in Israel and Ecuador revealed that despite their dwarfism and marked obesity, patients are alive at the ages of 75-78 years, with some having reached even more advanced ages.]. 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:18359741
;
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:NP862630.RA_gCYbQbs8Kw6R4Q_eqnuKtHfrTXh-rbtrT1QvIfbM1g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:47+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" .
}