@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP487780.RAApj9GBH0-4c0UyA8D9vWDre9NICEDzB7q-KN5MbckqE
> .
@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:NP487780.RAApj9GBH0-4c0UyA8D9vWDre9NICEDzB7q-KN5MbckqE130_head
{
this:
np:hasAssertion
dgn-np:NP487780.RAApj9GBH0-4c0UyA8D9vWDre9NICEDzB7q-KN5MbckqE130_assertion
;
np:hasProvenance
dgn-np:NP487780.RAApj9GBH0-4c0UyA8D9vWDre9NICEDzB7q-KN5MbckqE130_provenance
;
np:hasPublicationInfo
dgn-np:NP487780.RAApj9GBH0-4c0UyA8D9vWDre9NICEDzB7q-KN5MbckqE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP487780.RAApj9GBH0-4c0UyA8D9vWDre9NICEDzB7q-KN5MbckqE130_assertion
a
np:Assertion
.
dgn-np:NP487780.RAApj9GBH0-4c0UyA8D9vWDre9NICEDzB7q-KN5MbckqE130_provenance
a
np:Provenance
.
dgn-np:NP487780.RAApj9GBH0-4c0UyA8D9vWDre9NICEDzB7q-KN5MbckqE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP487780.RAApj9GBH0-4c0UyA8D9vWDre9NICEDzB7q-KN5MbckqE130_assertion
{
miriam-gene:1285
a
ncit:C16612
.
lld:C0017668
a
ncit:C7057
.
dgn-gda:DGN9fb1a302fe44a4b4181980ab8691def3
sio:SIO_000628
miriam-gene:1285
,
lld:C0017668
;
a
sio:SIO_001121
.
}
dgn-np:NP487780.RAApj9GBH0-4c0UyA8D9vWDre9NICEDzB7q-KN5MbckqE130_provenance
{
dgn-np:NP487780.RAApj9GBH0-4c0UyA8D9vWDre9NICEDzB7q-KN5MbckqE130_assertion
dcterms:description
"[We conclude that these particular COL4A3/COL4A4 mutations either predispose some patients to FSGS and chronic renal failure, or that thin basement membrane nephropathy sometimes coexists with another genetic modifier that is responsible for FSGS and progressive renal failure.]. 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:17942953
;
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:NP487780.RAApj9GBH0-4c0UyA8D9vWDre9NICEDzB7q-KN5MbckqE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:51+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" .
}