@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP383084.RA3CupmETm4tGGgerTFIneP7zx5rs2kEY6aFUnMdxL8a0
> .
@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:NP383084.RA3CupmETm4tGGgerTFIneP7zx5rs2kEY6aFUnMdxL8a0130_head
{
this:
np:hasAssertion
dgn-np:NP383084.RA3CupmETm4tGGgerTFIneP7zx5rs2kEY6aFUnMdxL8a0130_assertion
;
np:hasProvenance
dgn-np:NP383084.RA3CupmETm4tGGgerTFIneP7zx5rs2kEY6aFUnMdxL8a0130_provenance
;
np:hasPublicationInfo
dgn-np:NP383084.RA3CupmETm4tGGgerTFIneP7zx5rs2kEY6aFUnMdxL8a0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP383084.RA3CupmETm4tGGgerTFIneP7zx5rs2kEY6aFUnMdxL8a0130_assertion
a
np:Assertion
.
dgn-np:NP383084.RA3CupmETm4tGGgerTFIneP7zx5rs2kEY6aFUnMdxL8a0130_provenance
a
np:Provenance
.
dgn-np:NP383084.RA3CupmETm4tGGgerTFIneP7zx5rs2kEY6aFUnMdxL8a0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP383084.RA3CupmETm4tGGgerTFIneP7zx5rs2kEY6aFUnMdxL8a0130_assertion
{
miriam-gene:146
a
ncit:C16612
.
lld:C1567742
a
ncit:C7057
.
dgn-gda:DGN28e24132c807d0aa09ffc85d36cbffa4
sio:SIO_000628
miriam-gene:146
,
lld:C1567742
;
a
sio:SIO_001121
.
}
dgn-np:NP383084.RA3CupmETm4tGGgerTFIneP7zx5rs2kEY6aFUnMdxL8a0130_provenance
{
dgn-np:NP383084.RA3CupmETm4tGGgerTFIneP7zx5rs2kEY6aFUnMdxL8a0130_assertion
dcterms:description
"[COL4A5 mutations causing X-linked Alport syndrome (XLAS) are frequently associated with absence of the alpha3, alpha4,alpha5 and alpha6 chains of type IV collagen from basement membranes and increased amounts of the alpha1(IV) and alpha2(IV) chains in glomerular basement membrane.]. 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:9749944
;
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:NP383084.RA3CupmETm4tGGgerTFIneP7zx5rs2kEY6aFUnMdxL8a0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:48+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" .
}