@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP760509.RARUYLPas8xjAJJIAUmd_V-fBGzwV4HMOdo9bmn3E6tiw
> .
@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:NP760509.RARUYLPas8xjAJJIAUmd_V-fBGzwV4HMOdo9bmn3E6tiw130_head
{
this:
np:hasAssertion
dgn-np:NP760509.RARUYLPas8xjAJJIAUmd_V-fBGzwV4HMOdo9bmn3E6tiw130_assertion
;
np:hasProvenance
dgn-np:NP760509.RARUYLPas8xjAJJIAUmd_V-fBGzwV4HMOdo9bmn3E6tiw130_provenance
;
np:hasPublicationInfo
dgn-np:NP760509.RARUYLPas8xjAJJIAUmd_V-fBGzwV4HMOdo9bmn3E6tiw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP760509.RARUYLPas8xjAJJIAUmd_V-fBGzwV4HMOdo9bmn3E6tiw130_assertion
a
np:Assertion
.
dgn-np:NP760509.RARUYLPas8xjAJJIAUmd_V-fBGzwV4HMOdo9bmn3E6tiw130_provenance
a
np:Provenance
.
dgn-np:NP760509.RARUYLPas8xjAJJIAUmd_V-fBGzwV4HMOdo9bmn3E6tiw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP760509.RARUYLPas8xjAJJIAUmd_V-fBGzwV4HMOdo9bmn3E6tiw130_assertion
{
miriam-gene:7369
a
ncit:C16612
.
lld:C1868139
a
ncit:C7057
.
dgn-gda:DGNe6dce9c703b69103c8e3d986ac2953c0
sio:SIO_000628
miriam-gene:7369
,
lld:C1868139
;
a
sio:SIO_001121
.
}
dgn-np:NP760509.RARUYLPas8xjAJJIAUmd_V-fBGzwV4HMOdo9bmn3E6tiw130_provenance
{
dgn-np:NP760509.RARUYLPas8xjAJJIAUmd_V-fBGzwV4HMOdo9bmn3E6tiw130_assertion
dcterms:description
"[The location of a second genetic locus for autosomal dominant medullary cystic kidney disease (ADMCKD) at chromosome 16p12 led us to further investigate the molecular analysis of the critical region where two genes coding for uromodulin and SA proteins with renal specific functions, UMOD and SAH, are localized.]. 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:11730273
;
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:NP760509.RARUYLPas8xjAJJIAUmd_V-fBGzwV4HMOdo9bmn3E6tiw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:40+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" .
}