@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP320363.RAETX_lXh523KJ6CsegoYB-_1jco09LTgRHpuB8UefccM
> .
@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:NP320363.RAETX_lXh523KJ6CsegoYB-_1jco09LTgRHpuB8UefccM130_head
{
this:
np:hasAssertion
dgn-np:NP320363.RAETX_lXh523KJ6CsegoYB-_1jco09LTgRHpuB8UefccM130_assertion
;
np:hasProvenance
dgn-np:NP320363.RAETX_lXh523KJ6CsegoYB-_1jco09LTgRHpuB8UefccM130_provenance
;
np:hasPublicationInfo
dgn-np:NP320363.RAETX_lXh523KJ6CsegoYB-_1jco09LTgRHpuB8UefccM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP320363.RAETX_lXh523KJ6CsegoYB-_1jco09LTgRHpuB8UefccM130_assertion
a
np:Assertion
.
dgn-np:NP320363.RAETX_lXh523KJ6CsegoYB-_1jco09LTgRHpuB8UefccM130_provenance
a
np:Provenance
.
dgn-np:NP320363.RAETX_lXh523KJ6CsegoYB-_1jco09LTgRHpuB8UefccM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP320363.RAETX_lXh523KJ6CsegoYB-_1jco09LTgRHpuB8UefccM130_assertion
{
miriam-gene:1286
a
ncit:C16612
.
lld:C1567741
a
ncit:C7057
.
dgn-gda:DGN43b948fb87362ee025fc809438cc2826
sio:SIO_000628
miriam-gene:1286
,
lld:C1567741
;
a
sio:SIO_001121
.
}
dgn-np:NP320363.RAETX_lXh523KJ6CsegoYB-_1jco09LTgRHpuB8UefccM130_provenance
{
dgn-np:NP320363.RAETX_lXh523KJ6CsegoYB-_1jco09LTgRHpuB8UefccM130_assertion
dcterms:description
"[Recent genetic studies indicate that Alport syndrome and thin glomerular basement membrane disease (TMD) may both be due to COL4A3, COL4A4, and COL4A5 mutations, but there is continuing uncertainty concerning the diagnosis and management of patients without classic family history and symptoms.]. 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:12203217
;
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:NP320363.RAETX_lXh523KJ6CsegoYB-_1jco09LTgRHpuB8UefccM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:05+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" .
}