@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP904016.RA0xK0MHtHj_ZFlA_Ai0U01iiMSFtN6Ugk0NEz94E6uqI
> .
@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:NP904016.RA0xK0MHtHj_ZFlA_Ai0U01iiMSFtN6Ugk0NEz94E6uqI130_head
{
this:
np:hasAssertion
dgn-np:NP904016.RA0xK0MHtHj_ZFlA_Ai0U01iiMSFtN6Ugk0NEz94E6uqI130_assertion
;
np:hasProvenance
dgn-np:NP904016.RA0xK0MHtHj_ZFlA_Ai0U01iiMSFtN6Ugk0NEz94E6uqI130_provenance
;
np:hasPublicationInfo
dgn-np:NP904016.RA0xK0MHtHj_ZFlA_Ai0U01iiMSFtN6Ugk0NEz94E6uqI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP904016.RA0xK0MHtHj_ZFlA_Ai0U01iiMSFtN6Ugk0NEz94E6uqI130_assertion
a
np:Assertion
.
dgn-np:NP904016.RA0xK0MHtHj_ZFlA_Ai0U01iiMSFtN6Ugk0NEz94E6uqI130_provenance
a
np:Provenance
.
dgn-np:NP904016.RA0xK0MHtHj_ZFlA_Ai0U01iiMSFtN6Ugk0NEz94E6uqI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP904016.RA0xK0MHtHj_ZFlA_Ai0U01iiMSFtN6Ugk0NEz94E6uqI130_assertion
{
miriam-gene:6473
a
ncit:C16612
.
lld:C0549306
a
ncit:C7057
.
dgn-gda:DGN9a52cfccd6778ce2c82d6b15bf26c24d
sio:SIO_000628
miriam-gene:6473
,
lld:C0549306
;
a
sio:SIO_001121
.
}
dgn-np:NP904016.RA0xK0MHtHj_ZFlA_Ai0U01iiMSFtN6Ugk0NEz94E6uqI130_provenance
{
dgn-np:NP904016.RA0xK0MHtHj_ZFlA_Ai0U01iiMSFtN6Ugk0NEz94E6uqI130_assertion
dcterms:description
"[The results suggest that, in individuals with SHOX haploinsufficiency and normal ovarian function, auxological abnormalities related to mesomelia are evident from childhood and worsen further during puberty because of the skeletal maturing effects of ovarian estrogens.]. 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:14514349
;
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:NP904016.RA0xK0MHtHj_ZFlA_Ai0U01iiMSFtN6Ugk0NEz94E6uqI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:15+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" .
}