@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP780592.RAEzUPvMbjVuGrxs-CLEpj1972I61bMG3lVDH1WgzE96o
> .
@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:NP780592.RAEzUPvMbjVuGrxs-CLEpj1972I61bMG3lVDH1WgzE96o130_head
{
this:
np:hasAssertion
dgn-np:NP780592.RAEzUPvMbjVuGrxs-CLEpj1972I61bMG3lVDH1WgzE96o130_assertion
;
np:hasProvenance
dgn-np:NP780592.RAEzUPvMbjVuGrxs-CLEpj1972I61bMG3lVDH1WgzE96o130_provenance
;
np:hasPublicationInfo
dgn-np:NP780592.RAEzUPvMbjVuGrxs-CLEpj1972I61bMG3lVDH1WgzE96o130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP780592.RAEzUPvMbjVuGrxs-CLEpj1972I61bMG3lVDH1WgzE96o130_assertion
a
np:Assertion
.
dgn-np:NP780592.RAEzUPvMbjVuGrxs-CLEpj1972I61bMG3lVDH1WgzE96o130_provenance
a
np:Provenance
.
dgn-np:NP780592.RAEzUPvMbjVuGrxs-CLEpj1972I61bMG3lVDH1WgzE96o130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP780592.RAEzUPvMbjVuGrxs-CLEpj1972I61bMG3lVDH1WgzE96o130_assertion
{
miriam-gene:1287
a
ncit:C16612
.
lld:C0017636
a
ncit:C7057
.
dgn-gda:DGNe3ac6543d1d0fb873af9c2d08e27fe84
sio:SIO_000628
miriam-gene:1287
,
lld:C0017636
;
a
sio:SIO_001121
.
}
dgn-np:NP780592.RAEzUPvMbjVuGrxs-CLEpj1972I61bMG3lVDH1WgzE96o130_provenance
{
dgn-np:NP780592.RAEzUPvMbjVuGrxs-CLEpj1972I61bMG3lVDH1WgzE96o130_assertion
dcterms:description
"[Mutations in the COL4A5 gene encoding the alpha 5 chain of Type IV collagen were identified in three men with Alport syndrome and posttransplant antiglomerular basement membrane (GBM) nephritis by the use of Southern analysis, polymerase chain reaction amplification of genomic DNA, and reverse transcription and amplification of lymphocyte RNA.]. 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:7993995
;
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:NP780592.RAEzUPvMbjVuGrxs-CLEpj1972I61bMG3lVDH1WgzE96o130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:53+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" .
}