@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP324386.RAR3qkmEBl5ZrLpZr3_l5115lp-hJ0YkfXQBSbbOvyxVo
> .
@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:NP324386.RAR3qkmEBl5ZrLpZr3_l5115lp-hJ0YkfXQBSbbOvyxVo130_head
{
this:
np:hasAssertion
dgn-np:NP324386.RAR3qkmEBl5ZrLpZr3_l5115lp-hJ0YkfXQBSbbOvyxVo130_assertion
;
np:hasProvenance
dgn-np:NP324386.RAR3qkmEBl5ZrLpZr3_l5115lp-hJ0YkfXQBSbbOvyxVo130_provenance
;
np:hasPublicationInfo
dgn-np:NP324386.RAR3qkmEBl5ZrLpZr3_l5115lp-hJ0YkfXQBSbbOvyxVo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP324386.RAR3qkmEBl5ZrLpZr3_l5115lp-hJ0YkfXQBSbbOvyxVo130_assertion
a
np:Assertion
.
dgn-np:NP324386.RAR3qkmEBl5ZrLpZr3_l5115lp-hJ0YkfXQBSbbOvyxVo130_provenance
a
np:Provenance
.
dgn-np:NP324386.RAR3qkmEBl5ZrLpZr3_l5115lp-hJ0YkfXQBSbbOvyxVo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP324386.RAR3qkmEBl5ZrLpZr3_l5115lp-hJ0YkfXQBSbbOvyxVo130_assertion
{
miriam-gene:3480
a
ncit:C16612
.
lld:C0015544
a
ncit:C7057
.
dgn-gda:DGNfcd62a0cbabb306d8e127913db2d8875
sio:SIO_000628
miriam-gene:3480
,
lld:C0015544
;
a
sio:SIO_001121
.
}
dgn-np:NP324386.RAR3qkmEBl5ZrLpZr3_l5115lp-hJ0YkfXQBSbbOvyxVo130_provenance
{
dgn-np:NP324386.RAR3qkmEBl5ZrLpZr3_l5115lp-hJ0YkfXQBSbbOvyxVo130_assertion
dcterms:description
"[Three patients who had suffered severe growth failure in early childhood were hemizygous at the IGF1R locus, while one patient with borderline short stature had two copies of the IGF1R gene.]. 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:7789178
;
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:NP324386.RAR3qkmEBl5ZrLpZr3_l5115lp-hJ0YkfXQBSbbOvyxVo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:09+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" .
}