@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI
> .
@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:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_head
{
this:
np:hasAssertion
dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_assertion
;
np:hasProvenance
dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_provenance
;
np:hasPublicationInfo
dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_assertion
a
np:Assertion
.
dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_provenance
a
np:Provenance
.
dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_assertion
{
miriam-gene:5589
a
ncit:C16612
.
lld:C0022680
a
ncit:C7057
.
dgn-gda:DGN4f0e86034ecdd8ae4f8ff369efde64f0
sio:SIO_000628
miriam-gene:5589
,
lld:C0022680
;
a
sio:SIO_001121
.
}
dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_provenance
{
dgn-np:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_assertion
dcterms:description
"[PCLD exhibits both autosomal or recessive dominant pattern of inheritance and is characterized by the progressive development of multiple cysts, isolated or associated with polycystic kidney disease, that appear more extensive in women.]. 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:20138815
;
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:NP778133.RAMC8boDVJi_PVCPUXuW2SQfgf1LQO6JRxzjA2hwODCJI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:51+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" .
}