@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP792135.RAb0eIHQeioW7OohPjiqJxuoBgHFsoC66UH-ZvTazzdzA
> .
@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:NP792135.RAb0eIHQeioW7OohPjiqJxuoBgHFsoC66UH-ZvTazzdzA130_head
{
this:
np:hasAssertion
dgn-np:NP792135.RAb0eIHQeioW7OohPjiqJxuoBgHFsoC66UH-ZvTazzdzA130_assertion
;
np:hasProvenance
dgn-np:NP792135.RAb0eIHQeioW7OohPjiqJxuoBgHFsoC66UH-ZvTazzdzA130_provenance
;
np:hasPublicationInfo
dgn-np:NP792135.RAb0eIHQeioW7OohPjiqJxuoBgHFsoC66UH-ZvTazzdzA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP792135.RAb0eIHQeioW7OohPjiqJxuoBgHFsoC66UH-ZvTazzdzA130_assertion
a
np:Assertion
.
dgn-np:NP792135.RAb0eIHQeioW7OohPjiqJxuoBgHFsoC66UH-ZvTazzdzA130_provenance
a
np:Provenance
.
dgn-np:NP792135.RAb0eIHQeioW7OohPjiqJxuoBgHFsoC66UH-ZvTazzdzA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP792135.RAb0eIHQeioW7OohPjiqJxuoBgHFsoC66UH-ZvTazzdzA130_assertion
{
miriam-gene:6473
a
ncit:C16612
.
lld:C0878787
a
ncit:C7057
.
dgn-gda:DGN5ca2181f660f7d29d45ccaf77a979fcc
sio:SIO_000628
miriam-gene:6473
,
lld:C0878787
;
a
sio:SIO_001121
.
}
dgn-np:NP792135.RAb0eIHQeioW7OohPjiqJxuoBgHFsoC66UH-ZvTazzdzA130_provenance
{
dgn-np:NP792135.RAb0eIHQeioW7OohPjiqJxuoBgHFsoC66UH-ZvTazzdzA130_assertion
dcterms:description
"[The aim of this study was to determine the prevalence of SHOX mutations in LWD and to investigate the degree of growth failure in relation to mutation, sex, age of menarche, and wrist deformity.]. 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:15356038
;
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:NP792135.RAb0eIHQeioW7OohPjiqJxuoBgHFsoC66UH-ZvTazzdzA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:06+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" .
}