@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP886385.RAueHn4Uj2SyFl9Qi6LD0qv2jJTKupeTlZi3y5VgndUMo
> .
@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:NP886385.RAueHn4Uj2SyFl9Qi6LD0qv2jJTKupeTlZi3y5VgndUMo130_head
{
this:
np:hasAssertion
dgn-np:NP886385.RAueHn4Uj2SyFl9Qi6LD0qv2jJTKupeTlZi3y5VgndUMo130_assertion
;
np:hasProvenance
dgn-np:NP886385.RAueHn4Uj2SyFl9Qi6LD0qv2jJTKupeTlZi3y5VgndUMo130_provenance
;
np:hasPublicationInfo
dgn-np:NP886385.RAueHn4Uj2SyFl9Qi6LD0qv2jJTKupeTlZi3y5VgndUMo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP886385.RAueHn4Uj2SyFl9Qi6LD0qv2jJTKupeTlZi3y5VgndUMo130_assertion
a
np:Assertion
.
dgn-np:NP886385.RAueHn4Uj2SyFl9Qi6LD0qv2jJTKupeTlZi3y5VgndUMo130_provenance
a
np:Provenance
.
dgn-np:NP886385.RAueHn4Uj2SyFl9Qi6LD0qv2jJTKupeTlZi3y5VgndUMo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP886385.RAueHn4Uj2SyFl9Qi6LD0qv2jJTKupeTlZi3y5VgndUMo130_assertion
{
miriam-gene:2668
a
ncit:C16612
.
lld:C1609433
a
ncit:C7057
.
dgn-gda:DGNa7b6b950523c17ea0b2f5ad239834cb2
sio:SIO_000628
miriam-gene:2668
,
lld:C1609433
;
a
sio:SIO_001121
.
}
dgn-np:NP886385.RAueHn4Uj2SyFl9Qi6LD0qv2jJTKupeTlZi3y5VgndUMo130_provenance
{
dgn-np:NP886385.RAueHn4Uj2SyFl9Qi6LD0qv2jJTKupeTlZi3y5VgndUMo130_assertion
dcterms:description
"[Individual or a combination of GDNF, RET and SPRY1 mutant alleles in mice cause renal malformations reminiscent of congenital anomalies of the kidney or urinary tract (CAKUT) in humans and distinct from renal agenesis phenotype in complete GDNF or RET-null mice.]. 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:22729463
;
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:NP886385.RAueHn4Uj2SyFl9Qi6LD0qv2jJTKupeTlZi3y5VgndUMo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:01+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: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" .
}