@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1358112.RAl2Kl2QxQDflS8_rghMRLw35Hy6eVsa5VQsXX4YD8mqE
> .
@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/v4.0.0/void/
> .
dgn-np:NP1358112.RAl2Kl2QxQDflS8_rghMRLw35Hy6eVsa5VQsXX4YD8mqE130_head
{
this:
np:hasAssertion
dgn-np:NP1358112.RAl2Kl2QxQDflS8_rghMRLw35Hy6eVsa5VQsXX4YD8mqE130_assertion
;
np:hasProvenance
dgn-np:NP1358112.RAl2Kl2QxQDflS8_rghMRLw35Hy6eVsa5VQsXX4YD8mqE130_provenance
;
np:hasPublicationInfo
dgn-np:NP1358112.RAl2Kl2QxQDflS8_rghMRLw35Hy6eVsa5VQsXX4YD8mqE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1358112.RAl2Kl2QxQDflS8_rghMRLw35Hy6eVsa5VQsXX4YD8mqE130_assertion
a
np:Assertion
.
dgn-np:NP1358112.RAl2Kl2QxQDflS8_rghMRLw35Hy6eVsa5VQsXX4YD8mqE130_provenance
a
np:Provenance
.
dgn-np:NP1358112.RAl2Kl2QxQDflS8_rghMRLw35Hy6eVsa5VQsXX4YD8mqE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1358112.RAl2Kl2QxQDflS8_rghMRLw35Hy6eVsa5VQsXX4YD8mqE130_assertion
{
miriam-gene:5745
a
ncit:C16612
.
lld:C0265290
a
ncit:C7057
.
dgn-gda:DGN97fe025b25b2dd1ca681df0e5d08baee
sio:SIO_000628
miriam-gene:5745
,
lld:C0265290
;
a
sio:SIO_001121
.
}
dgn-np:NP1358112.RAl2Kl2QxQDflS8_rghMRLw35Hy6eVsa5VQsXX4YD8mqE130_provenance
{
dgn-np:NP1358112.RAl2Kl2QxQDflS8_rghMRLw35Hy6eVsa5VQsXX4YD8mqE130_assertion
dcterms:description
"[To search for human diseases that are caused by parathyroid hormone/parathyroid hormone-related peptide receptor defects, genomic DNA of patients with pseudohypoparathyroidism type Ib and of patients with Jansen's metaphyseal chondrodysplasia was screened for mutations in all coding exons of the receptor gene.]. 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:8823526
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1358112.RAl2Kl2QxQDflS8_rghMRLw35Hy6eVsa5VQsXX4YD8mqE130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:01+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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}