@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP410828.RA6pbm3nfQjY8vHcMoDupsXWGI0MuwDiWu9ktDeGC9IoU
> .
@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:NP410828.RA6pbm3nfQjY8vHcMoDupsXWGI0MuwDiWu9ktDeGC9IoU130_head
{
this:
np:hasAssertion
dgn-np:NP410828.RA6pbm3nfQjY8vHcMoDupsXWGI0MuwDiWu9ktDeGC9IoU130_assertion
;
np:hasProvenance
dgn-np:NP410828.RA6pbm3nfQjY8vHcMoDupsXWGI0MuwDiWu9ktDeGC9IoU130_provenance
;
np:hasPublicationInfo
dgn-np:NP410828.RA6pbm3nfQjY8vHcMoDupsXWGI0MuwDiWu9ktDeGC9IoU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP410828.RA6pbm3nfQjY8vHcMoDupsXWGI0MuwDiWu9ktDeGC9IoU130_assertion
a
np:Assertion
.
dgn-np:NP410828.RA6pbm3nfQjY8vHcMoDupsXWGI0MuwDiWu9ktDeGC9IoU130_provenance
a
np:Provenance
.
dgn-np:NP410828.RA6pbm3nfQjY8vHcMoDupsXWGI0MuwDiWu9ktDeGC9IoU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP410828.RA6pbm3nfQjY8vHcMoDupsXWGI0MuwDiWu9ktDeGC9IoU130_assertion
{
miriam-gene:1288
a
ncit:C16612
.
lld:C1567742
a
ncit:C7057
.
dgn-gda:DGNacc6453c6bc4fda6d755802488872ff2
sio:SIO_000628
miriam-gene:1288
,
lld:C1567742
;
a
sio:SIO_001121
.
}
dgn-np:NP410828.RA6pbm3nfQjY8vHcMoDupsXWGI0MuwDiWu9ktDeGC9IoU130_provenance
{
dgn-np:NP410828.RA6pbm3nfQjY8vHcMoDupsXWGI0MuwDiWu9ktDeGC9IoU130_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-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:NP410828.RA6pbm3nfQjY8vHcMoDupsXWGI0MuwDiWu9ktDeGC9IoU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:04+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" .
}