@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP440732.RAioQfHYSEGViTz0aT4FCOoZgBqMYnGU8WqO5auu9dsf0
> .
@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:NP440732.RAioQfHYSEGViTz0aT4FCOoZgBqMYnGU8WqO5auu9dsf0130_head
{
this:
np:hasAssertion
dgn-np:NP440732.RAioQfHYSEGViTz0aT4FCOoZgBqMYnGU8WqO5auu9dsf0130_assertion
;
np:hasProvenance
dgn-np:NP440732.RAioQfHYSEGViTz0aT4FCOoZgBqMYnGU8WqO5auu9dsf0130_provenance
;
np:hasPublicationInfo
dgn-np:NP440732.RAioQfHYSEGViTz0aT4FCOoZgBqMYnGU8WqO5auu9dsf0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP440732.RAioQfHYSEGViTz0aT4FCOoZgBqMYnGU8WqO5auu9dsf0130_assertion
a
np:Assertion
.
dgn-np:NP440732.RAioQfHYSEGViTz0aT4FCOoZgBqMYnGU8WqO5auu9dsf0130_provenance
a
np:Provenance
.
dgn-np:NP440732.RAioQfHYSEGViTz0aT4FCOoZgBqMYnGU8WqO5auu9dsf0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP440732.RAioQfHYSEGViTz0aT4FCOoZgBqMYnGU8WqO5auu9dsf0130_assertion
{
miriam-gene:8542
a
ncit:C16612
.
lld:C0022658
a
ncit:C7057
.
dgn-gda:DGNe6414bdcd88a1b8526c4013462821a97
sio:SIO_000628
miriam-gene:8542
,
lld:C0022658
;
a
sio:SIO_001121
.
}
dgn-np:NP440732.RAioQfHYSEGViTz0aT4FCOoZgBqMYnGU8WqO5auu9dsf0130_provenance
{
dgn-np:NP440732.RAioQfHYSEGViTz0aT4FCOoZgBqMYnGU8WqO5auu9dsf0130_assertion
dcterms:description
"[We review evidence that MYH9 dysfunction in humans results in similar susceptibility and place our data, the first examination of Myh9 kidney disease in experimental animals, in the context of recent findings in human kidney disease, including the role of APOL1.]. 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:21402784
;
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:NP440732.RAioQfHYSEGViTz0aT4FCOoZgBqMYnGU8WqO5auu9dsf0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:20+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" .
}