@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1346744.RAucdNbElHnjr9259MqH8WodAy_b3V53tOhclhHUJdVY8
> .
@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:NP1346744.RAucdNbElHnjr9259MqH8WodAy_b3V53tOhclhHUJdVY8130_head
{
this:
np:hasAssertion
dgn-np:NP1346744.RAucdNbElHnjr9259MqH8WodAy_b3V53tOhclhHUJdVY8130_assertion
;
np:hasProvenance
dgn-np:NP1346744.RAucdNbElHnjr9259MqH8WodAy_b3V53tOhclhHUJdVY8130_provenance
;
np:hasPublicationInfo
dgn-np:NP1346744.RAucdNbElHnjr9259MqH8WodAy_b3V53tOhclhHUJdVY8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1346744.RAucdNbElHnjr9259MqH8WodAy_b3V53tOhclhHUJdVY8130_assertion
a
np:Assertion
.
dgn-np:NP1346744.RAucdNbElHnjr9259MqH8WodAy_b3V53tOhclhHUJdVY8130_provenance
a
np:Provenance
.
dgn-np:NP1346744.RAucdNbElHnjr9259MqH8WodAy_b3V53tOhclhHUJdVY8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1346744.RAucdNbElHnjr9259MqH8WodAy_b3V53tOhclhHUJdVY8130_assertion
{
miriam-gene:1287
a
ncit:C16612
.
lld:C1567742
a
ncit:C7057
.
dgn-gda:DGNc4c3e9db1e61f1acc90b4f71eb2a2401
sio:SIO_000628
miriam-gene:1287
,
lld:C1567742
;
a
sio:SIO_001121
.
}
dgn-np:NP1346744.RAucdNbElHnjr9259MqH8WodAy_b3V53tOhclhHUJdVY8130_provenance
{
dgn-np:NP1346744.RAucdNbElHnjr9259MqH8WodAy_b3V53tOhclhHUJdVY8130_assertion
dcterms:description
"[X-linked Alport syndrome (AS) associated with diffuse esophageal leiomyomatosis (DL) has been reported to be due to deletions removing the 5' ends of both the COL4A5 and COL4A6 genes, encoding the alpha 5 and alpha 6 chains of type IV collagen, respectively, whereas a variety of mutations in COL4A5 has been identified in patients with AS alone.]. 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:8587250
;
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:NP1346744.RAucdNbElHnjr9259MqH8WodAy_b3V53tOhclhHUJdVY8130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:56+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" .
}