@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP936800.RAvN50loi-0M_aaYDEfPH9-7A2LCMXV5S6VQibYhpySVU
> .
@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:NP936800.RAvN50loi-0M_aaYDEfPH9-7A2LCMXV5S6VQibYhpySVU130_head
{
this:
np:hasAssertion
dgn-np:NP936800.RAvN50loi-0M_aaYDEfPH9-7A2LCMXV5S6VQibYhpySVU130_assertion
;
np:hasProvenance
dgn-np:NP936800.RAvN50loi-0M_aaYDEfPH9-7A2LCMXV5S6VQibYhpySVU130_provenance
;
np:hasPublicationInfo
dgn-np:NP936800.RAvN50loi-0M_aaYDEfPH9-7A2LCMXV5S6VQibYhpySVU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP936800.RAvN50loi-0M_aaYDEfPH9-7A2LCMXV5S6VQibYhpySVU130_assertion
a
np:Assertion
.
dgn-np:NP936800.RAvN50loi-0M_aaYDEfPH9-7A2LCMXV5S6VQibYhpySVU130_provenance
a
np:Provenance
.
dgn-np:NP936800.RAvN50loi-0M_aaYDEfPH9-7A2LCMXV5S6VQibYhpySVU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP936800.RAvN50loi-0M_aaYDEfPH9-7A2LCMXV5S6VQibYhpySVU130_assertion
{
miriam-gene:2182
a
ncit:C16612
.
lld:C1567741
a
ncit:C7057
.
dgn-gda:DGNcd5e0a79f475fc0f6b33141d59e4a355
sio:SIO_000628
miriam-gene:2182
,
lld:C1567741
;
a
sio:SIO_001121
.
}
dgn-np:NP936800.RAvN50loi-0M_aaYDEfPH9-7A2LCMXV5S6VQibYhpySVU130_provenance
{
dgn-np:NP936800.RAvN50loi-0M_aaYDEfPH9-7A2LCMXV5S6VQibYhpySVU130_assertion
dcterms:description
"[While the Alport syndrome is due to deletion of the COL4A5 gene, no other genes are known in the region with the exception of our recent finding of the FACL4 gene.]. 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:10049589
;
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:NP936800.RAvN50loi-0M_aaYDEfPH9-7A2LCMXV5S6VQibYhpySVU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:34+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" .
}