@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP788251.RA8l4DTzh9lZFAre-kk-ouuc5WE-2xN_7ovRSy9V7gc-Y
> .
@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/v3.0.0/void/
> .
dgn-np:NP788251.RA8l4DTzh9lZFAre-kk-ouuc5WE-2xN_7ovRSy9V7gc-Y130_head
{
this:
np:hasAssertion
dgn-np:NP788251.RA8l4DTzh9lZFAre-kk-ouuc5WE-2xN_7ovRSy9V7gc-Y130_assertion
;
np:hasProvenance
dgn-np:NP788251.RA8l4DTzh9lZFAre-kk-ouuc5WE-2xN_7ovRSy9V7gc-Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP788251.RA8l4DTzh9lZFAre-kk-ouuc5WE-2xN_7ovRSy9V7gc-Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP788251.RA8l4DTzh9lZFAre-kk-ouuc5WE-2xN_7ovRSy9V7gc-Y130_assertion
a
np:Assertion
.
dgn-np:NP788251.RA8l4DTzh9lZFAre-kk-ouuc5WE-2xN_7ovRSy9V7gc-Y130_provenance
a
np:Provenance
.
dgn-np:NP788251.RA8l4DTzh9lZFAre-kk-ouuc5WE-2xN_7ovRSy9V7gc-Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP788251.RA8l4DTzh9lZFAre-kk-ouuc5WE-2xN_7ovRSy9V7gc-Y130_assertion
{
miriam-gene:8022
a
ncit:C16612
.
lld:C0013338
a
ncit:C7057
.
dgn-gda:DGN41d0f67b68f79d4cd5148762b79c32c7
sio:SIO_000628
miriam-gene:8022
,
lld:C0013338
;
a
sio:SIO_001122
.
}
dgn-np:NP788251.RA8l4DTzh9lZFAre-kk-ouuc5WE-2xN_7ovRSy9V7gc-Y130_provenance
{
dgn-np:NP788251.RA8l4DTzh9lZFAre-kk-ouuc5WE-2xN_7ovRSy9V7gc-Y130_assertion
dcterms:description
"[The objective of the study was to determine the frequency and nature of LHX3 mutations in patients with isolated GH deficiency or combined pituitary hormone deficiency (CPHD) and characterize the molecular consequences of mutations.]. 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:17327381
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP788251.RA8l4DTzh9lZFAre-kk-ouuc5WE-2xN_7ovRSy9V7gc-Y130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:36+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}