@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP724388.RAiPSTrOUd9CoEEMnUT8mkIT2gRSbHCOaCcJUgByiwtbo
> .
@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:NP724388.RAiPSTrOUd9CoEEMnUT8mkIT2gRSbHCOaCcJUgByiwtbo130_head
{
this:
np:hasAssertion
dgn-np:NP724388.RAiPSTrOUd9CoEEMnUT8mkIT2gRSbHCOaCcJUgByiwtbo130_assertion
;
np:hasProvenance
dgn-np:NP724388.RAiPSTrOUd9CoEEMnUT8mkIT2gRSbHCOaCcJUgByiwtbo130_provenance
;
np:hasPublicationInfo
dgn-np:NP724388.RAiPSTrOUd9CoEEMnUT8mkIT2gRSbHCOaCcJUgByiwtbo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP724388.RAiPSTrOUd9CoEEMnUT8mkIT2gRSbHCOaCcJUgByiwtbo130_assertion
a
np:Assertion
.
dgn-np:NP724388.RAiPSTrOUd9CoEEMnUT8mkIT2gRSbHCOaCcJUgByiwtbo130_provenance
a
np:Provenance
.
dgn-np:NP724388.RAiPSTrOUd9CoEEMnUT8mkIT2gRSbHCOaCcJUgByiwtbo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP724388.RAiPSTrOUd9CoEEMnUT8mkIT2gRSbHCOaCcJUgByiwtbo130_assertion
{
miriam-gene:1286
a
ncit:C16612
.
lld:C0017658
a
ncit:C7057
.
dgn-gda:DGN09959634ea05e53438f3c321fd7daf10
sio:SIO_000628
miriam-gene:1286
,
lld:C0017658
;
a
sio:SIO_001121
.
}
dgn-np:NP724388.RAiPSTrOUd9CoEEMnUT8mkIT2gRSbHCOaCcJUgByiwtbo130_provenance
{
dgn-np:NP724388.RAiPSTrOUd9CoEEMnUT8mkIT2gRSbHCOaCcJUgByiwtbo130_assertion
dcterms:description
"[Autosomal recessive Alport syndrome is a progressive hematuric glomerulonephritis characterized by glomerular basement membrane abnormalities and associated with mutations in either the COL4A3 or the COL4A4 gene, which encode the alpha3 and alpha4 type IV collagen chains, respectively.]. 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:9792860
;
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:NP724388.RAiPSTrOUd9CoEEMnUT8mkIT2gRSbHCOaCcJUgByiwtbo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:19+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" .
}