@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP489345.RADXXAprUkpA85n0LiG0TcEkZuiC6K3b3zv4ubWm1b-RM
> .
@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:NP489345.RADXXAprUkpA85n0LiG0TcEkZuiC6K3b3zv4ubWm1b-RM130_head
{
this:
np:hasAssertion
dgn-np:NP489345.RADXXAprUkpA85n0LiG0TcEkZuiC6K3b3zv4ubWm1b-RM130_assertion
;
np:hasProvenance
dgn-np:NP489345.RADXXAprUkpA85n0LiG0TcEkZuiC6K3b3zv4ubWm1b-RM130_provenance
;
np:hasPublicationInfo
dgn-np:NP489345.RADXXAprUkpA85n0LiG0TcEkZuiC6K3b3zv4ubWm1b-RM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP489345.RADXXAprUkpA85n0LiG0TcEkZuiC6K3b3zv4ubWm1b-RM130_assertion
a
np:Assertion
.
dgn-np:NP489345.RADXXAprUkpA85n0LiG0TcEkZuiC6K3b3zv4ubWm1b-RM130_provenance
a
np:Provenance
.
dgn-np:NP489345.RADXXAprUkpA85n0LiG0TcEkZuiC6K3b3zv4ubWm1b-RM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP489345.RADXXAprUkpA85n0LiG0TcEkZuiC6K3b3zv4ubWm1b-RM130_assertion
{
miriam-gene:213
a
ncit:C16612
.
lld:C0011860
a
ncit:C7057
.
dgn-gda:DGN4e485ff9495bcb003c88319bb66ff9ed
sio:SIO_000628
miriam-gene:213
,
lld:C0011860
;
a
sio:SIO_001121
.
}
dgn-np:NP489345.RADXXAprUkpA85n0LiG0TcEkZuiC6K3b3zv4ubWm1b-RM130_provenance
{
dgn-np:NP489345.RADXXAprUkpA85n0LiG0TcEkZuiC6K3b3zv4ubWm1b-RM130_assertion
dcterms:description
"[By use of genome-scan approaches, several research groups have identified genetic regions on chromosomes 7q, 18q, and 22q that harbor genes that determine either variation in urinary albumin excretion or susceptibility to proteinuria in families who have type 2 diabetes.]. 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:15822051
;
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:NP489345.RADXXAprUkpA85n0LiG0TcEkZuiC6K3b3zv4ubWm1b-RM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:26+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" .
}