@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k
> .
@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:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_head
{
this:
np:hasAssertion
dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_assertion
;
np:hasProvenance
dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_provenance
;
np:hasPublicationInfo
dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_assertion
a
np:Assertion
.
dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_provenance
a
np:Provenance
.
dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_assertion
{
miriam-gene:2688
a
ncit:C16612
.
lld:C0744483
a
ncit:C7057
.
dgn-gda:DGNfb0f06bdb60c1083a685bad7e14daf90
sio:SIO_000628
miriam-gene:2688
,
lld:C0744483
;
a
sio:SIO_001121
.
}
dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_provenance
{
dgn-np:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_assertion
dcterms:description
"[We report a boy with anhidrotic/hypohidrotic ectodermal dysplasia and growth hormone neurosecretory dysfunction, an association not previously reported, and we discuss the possible causes as well as the patient's response to growth hormone treatment until he reached final height.]. 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:19960895
;
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:NP591193.RAjsOARX69u6qsfwtNsCcf402mc_0GzwOl7LFjyL2WU5k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:55+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" .
}