@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU
> .
@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:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_head
{
this:
np:hasAssertion
dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_assertion
;
np:hasProvenance
dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_provenance
;
np:hasPublicationInfo
dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_assertion
a
np:Assertion
.
dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_provenance
a
np:Provenance
.
dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_assertion
{
miriam-gene:8022
a
ncit:C16612
.
lld:C0599750
a
ncit:C7057
.
dgn-gda:DGNad7e8c34f75bfbd56a45d96bc411a185
sio:SIO_000628
miriam-gene:8022
,
lld:C0599750
;
a
sio:SIO_001121
.
}
dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_provenance
{
dgn-np:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_assertion
dcterms:description
"[All patients were homozygous, with various syndromic forms of combined pituitary hormone deficiency (CPHD), hampering to allocate, in these consanguineous patients, the respective contribution of LHX3 and additional genes to each symptom.]. 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:22238406
;
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:NP246035.RAdQwiZ1lW94daRZug_Jum812M2dGkEMa9JKw4oiVpyUU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:17+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" .
}