@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP543767.RA3czowUkzGJLbQIeBhuv9OoaQRrJqd0RmXBGRAXr1YAw
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP543767.RA3czowUkzGJLbQIeBhuv9OoaQRrJqd0RmXBGRAXr1YAw130_head
{
this:
np:hasAssertion
dgn-np:NP543767.RA3czowUkzGJLbQIeBhuv9OoaQRrJqd0RmXBGRAXr1YAw130_assertion
;
np:hasProvenance
dgn-np:NP543767.RA3czowUkzGJLbQIeBhuv9OoaQRrJqd0RmXBGRAXr1YAw130_provenance
;
np:hasPublicationInfo
dgn-np:NP543767.RA3czowUkzGJLbQIeBhuv9OoaQRrJqd0RmXBGRAXr1YAw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP543767.RA3czowUkzGJLbQIeBhuv9OoaQRrJqd0RmXBGRAXr1YAw130_assertion
a
np:Assertion
.
dgn-np:NP543767.RA3czowUkzGJLbQIeBhuv9OoaQRrJqd0RmXBGRAXr1YAw130_provenance
a
np:Provenance
.
dgn-np:NP543767.RA3czowUkzGJLbQIeBhuv9OoaQRrJqd0RmXBGRAXr1YAw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP543767.RA3czowUkzGJLbQIeBhuv9OoaQRrJqd0RmXBGRAXr1YAw130_assertion
{
miriam-gene:6473
a
ncit:C16612
.
lld:C0265309
a
ncit:C7057
.
dgn-gda:DGN88ee53c5f97ddc450dfac82c71ca4297
sio:SIO_000628
miriam-gene:6473
,
lld:C0265309
;
a
sio:SIO_001121
.
}
dgn-np:NP543767.RA3czowUkzGJLbQIeBhuv9OoaQRrJqd0RmXBGRAXr1YAw130_provenance
{
dgn-np:NP543767.RA3czowUkzGJLbQIeBhuv9OoaQRrJqd0RmXBGRAXr1YAw130_assertion
dcterms:description
"[The high frequency of SHOX anomalies in the ISS group can be explained by the large proportion of boys in this group, reflecting the difficulty in diagnosing dyschondrosteosis in young boys.]. 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:16597678
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP543767.RA3czowUkzGJLbQIeBhuv9OoaQRrJqd0RmXBGRAXr1YAw130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:51+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}