@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP384358.RAR28nCjRi4phCYR9X7xvctploSaM5uKz1Rf9lrCy9das
> .
@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:NP384358.RAR28nCjRi4phCYR9X7xvctploSaM5uKz1Rf9lrCy9das130_head
{
this:
np:hasAssertion
dgn-np:NP384358.RAR28nCjRi4phCYR9X7xvctploSaM5uKz1Rf9lrCy9das130_assertion
;
np:hasProvenance
dgn-np:NP384358.RAR28nCjRi4phCYR9X7xvctploSaM5uKz1Rf9lrCy9das130_provenance
;
np:hasPublicationInfo
dgn-np:NP384358.RAR28nCjRi4phCYR9X7xvctploSaM5uKz1Rf9lrCy9das130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP384358.RAR28nCjRi4phCYR9X7xvctploSaM5uKz1Rf9lrCy9das130_assertion
a
np:Assertion
.
dgn-np:NP384358.RAR28nCjRi4phCYR9X7xvctploSaM5uKz1Rf9lrCy9das130_provenance
a
np:Provenance
.
dgn-np:NP384358.RAR28nCjRi4phCYR9X7xvctploSaM5uKz1Rf9lrCy9das130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP384358.RAR28nCjRi4phCYR9X7xvctploSaM5uKz1Rf9lrCy9das130_assertion
{
miriam-gene:5741
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGNaec2000ec620a01dc776b14cd8be32ec
sio:SIO_000628
miriam-gene:5741
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP384358.RAR28nCjRi4phCYR9X7xvctploSaM5uKz1Rf9lrCy9das130_provenance
{
dgn-np:NP384358.RAR28nCjRi4phCYR9X7xvctploSaM5uKz1Rf9lrCy9das130_assertion
dcterms:description
"[Described originally by Fuller Albright and his colleagues in early 1940s, this rare genetic disease is subclassified into two types according to the nephrogenous response to the administration of biologically active PTH.]. 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:23392091
;
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:NP384358.RAR28nCjRi4phCYR9X7xvctploSaM5uKz1Rf9lrCy9das130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:49+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" .
}