@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP755938.RAhTFiol1RkKw0CWm_UrGsk4kMx2DXE2ZgkDyFGnGAYkA
> .
@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:NP755938.RAhTFiol1RkKw0CWm_UrGsk4kMx2DXE2ZgkDyFGnGAYkA130_head
{
this:
np:hasAssertion
dgn-np:NP755938.RAhTFiol1RkKw0CWm_UrGsk4kMx2DXE2ZgkDyFGnGAYkA130_assertion
;
np:hasProvenance
dgn-np:NP755938.RAhTFiol1RkKw0CWm_UrGsk4kMx2DXE2ZgkDyFGnGAYkA130_provenance
;
np:hasPublicationInfo
dgn-np:NP755938.RAhTFiol1RkKw0CWm_UrGsk4kMx2DXE2ZgkDyFGnGAYkA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP755938.RAhTFiol1RkKw0CWm_UrGsk4kMx2DXE2ZgkDyFGnGAYkA130_assertion
a
np:Assertion
.
dgn-np:NP755938.RAhTFiol1RkKw0CWm_UrGsk4kMx2DXE2ZgkDyFGnGAYkA130_provenance
a
np:Provenance
.
dgn-np:NP755938.RAhTFiol1RkKw0CWm_UrGsk4kMx2DXE2ZgkDyFGnGAYkA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP755938.RAhTFiol1RkKw0CWm_UrGsk4kMx2DXE2ZgkDyFGnGAYkA130_assertion
{
miriam-gene:7166
a
ncit:C16612
.
lld:C0005941
a
ncit:C7057
.
dgn-gda:DGNaa478f7679ab319133e891e948db1316
sio:SIO_000628
miriam-gene:7166
,
lld:C0005941
;
a
sio:SIO_001121
.
}
dgn-np:NP755938.RAhTFiol1RkKw0CWm_UrGsk4kMx2DXE2ZgkDyFGnGAYkA130_provenance
{
dgn-np:NP755938.RAhTFiol1RkKw0CWm_UrGsk4kMx2DXE2ZgkDyFGnGAYkA130_assertion
dcterms:description
"[We could not find disease-causing coding variants in neither of the tested genes and therefore, we cannot provide support for an important function of TPH1 and HTR1B in the pathogenesis of sclerosing bone dysplasias in our tested patient cohort.]. 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:23563356
;
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:NP755938.RAhTFiol1RkKw0CWm_UrGsk4kMx2DXE2ZgkDyFGnGAYkA130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:45:16+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" .
}