@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP921683.RAENEqeuybxrtddAUd3kY-GLB68dyMs2oIgeik4_oTAGE
> .
@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:NP921683.RAENEqeuybxrtddAUd3kY-GLB68dyMs2oIgeik4_oTAGE130_head
{
this:
np:hasAssertion
dgn-np:NP921683.RAENEqeuybxrtddAUd3kY-GLB68dyMs2oIgeik4_oTAGE130_assertion
;
np:hasProvenance
dgn-np:NP921683.RAENEqeuybxrtddAUd3kY-GLB68dyMs2oIgeik4_oTAGE130_provenance
;
np:hasPublicationInfo
dgn-np:NP921683.RAENEqeuybxrtddAUd3kY-GLB68dyMs2oIgeik4_oTAGE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP921683.RAENEqeuybxrtddAUd3kY-GLB68dyMs2oIgeik4_oTAGE130_assertion
a
np:Assertion
.
dgn-np:NP921683.RAENEqeuybxrtddAUd3kY-GLB68dyMs2oIgeik4_oTAGE130_provenance
a
np:Provenance
.
dgn-np:NP921683.RAENEqeuybxrtddAUd3kY-GLB68dyMs2oIgeik4_oTAGE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP921683.RAENEqeuybxrtddAUd3kY-GLB68dyMs2oIgeik4_oTAGE130_assertion
{
miriam-gene:1288
a
ncit:C16612
.
lld:C0035078
a
ncit:C7057
.
dgn-gda:DGNc59945a97cdb97a2c358bf282f3cf186
sio:SIO_000628
miriam-gene:1288
,
lld:C0035078
;
a
sio:SIO_001121
.
}
dgn-np:NP921683.RAENEqeuybxrtddAUd3kY-GLB68dyMs2oIgeik4_oTAGE130_provenance
{
dgn-np:NP921683.RAENEqeuybxrtddAUd3kY-GLB68dyMs2oIgeik4_oTAGE130_assertion
dcterms:description
"[The results indicate that mutations in COL4A5 that leading to renal failure are more frequent than those involved in classic Alport syndrome, and also that mutations in COL4A6 are not likely to cause this disease.]. 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:8738805
;
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:NP921683.RAENEqeuybxrtddAUd3kY-GLB68dyMs2oIgeik4_oTAGE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:25+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" .
}