@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1351687.RAUdqJmRj4ku2h2AkKfaMgEEdniP9ioAmd6FIOAsbNX_s
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1351687.RAUdqJmRj4ku2h2AkKfaMgEEdniP9ioAmd6FIOAsbNX_s130_head
{
this:
np:hasAssertion
dgn-np:NP1351687.RAUdqJmRj4ku2h2AkKfaMgEEdniP9ioAmd6FIOAsbNX_s130_assertion
;
np:hasProvenance
dgn-np:NP1351687.RAUdqJmRj4ku2h2AkKfaMgEEdniP9ioAmd6FIOAsbNX_s130_provenance
;
np:hasPublicationInfo
dgn-np:NP1351687.RAUdqJmRj4ku2h2AkKfaMgEEdniP9ioAmd6FIOAsbNX_s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1351687.RAUdqJmRj4ku2h2AkKfaMgEEdniP9ioAmd6FIOAsbNX_s130_assertion
a
np:Assertion
.
dgn-np:NP1351687.RAUdqJmRj4ku2h2AkKfaMgEEdniP9ioAmd6FIOAsbNX_s130_provenance
a
np:Provenance
.
dgn-np:NP1351687.RAUdqJmRj4ku2h2AkKfaMgEEdniP9ioAmd6FIOAsbNX_s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1351687.RAUdqJmRj4ku2h2AkKfaMgEEdniP9ioAmd6FIOAsbNX_s130_assertion
{
miriam-gene:1287
a
ncit:C16612
.
lld:C1567741
a
ncit:C7057
.
dgn-gda:DGNdaa42aafcfc9a5012405d44c53690978
sio:SIO_000628
miriam-gene:1287
,
lld:C1567741
;
a
sio:SIO_001121
.
}
dgn-np:NP1351687.RAUdqJmRj4ku2h2AkKfaMgEEdniP9ioAmd6FIOAsbNX_s130_provenance
{
dgn-np:NP1351687.RAUdqJmRj4ku2h2AkKfaMgEEdniP9ioAmd6FIOAsbNX_s130_assertion
dcterms:description
"[Patients with leimoyomatosis associated with Alport syndrome have been shown to have deletions in the 5' end of the COL4A6 gene, in addition to having deletions in COL4A5 (Zhou et al., Science 261: 1167-1169, 1993).]. 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:8661006
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1351687.RAUdqJmRj4ku2h2AkKfaMgEEdniP9ioAmd6FIOAsbNX_s130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:59+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}