@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP476850.RAQfbfFa8gy4kM0tKN_E66wEQfPtORedZdKZ64swl_ZYU
> .
@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:NP476850.RAQfbfFa8gy4kM0tKN_E66wEQfPtORedZdKZ64swl_ZYU130_head
{
this:
np:hasAssertion
dgn-np:NP476850.RAQfbfFa8gy4kM0tKN_E66wEQfPtORedZdKZ64swl_ZYU130_assertion
;
np:hasProvenance
dgn-np:NP476850.RAQfbfFa8gy4kM0tKN_E66wEQfPtORedZdKZ64swl_ZYU130_provenance
;
np:hasPublicationInfo
dgn-np:NP476850.RAQfbfFa8gy4kM0tKN_E66wEQfPtORedZdKZ64swl_ZYU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP476850.RAQfbfFa8gy4kM0tKN_E66wEQfPtORedZdKZ64swl_ZYU130_assertion
a
np:Assertion
.
dgn-np:NP476850.RAQfbfFa8gy4kM0tKN_E66wEQfPtORedZdKZ64swl_ZYU130_provenance
a
np:Provenance
.
dgn-np:NP476850.RAQfbfFa8gy4kM0tKN_E66wEQfPtORedZdKZ64swl_ZYU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP476850.RAQfbfFa8gy4kM0tKN_E66wEQfPtORedZdKZ64swl_ZYU130_assertion
{
miriam-gene:4627
a
ncit:C16612
.
lld:C0403434
a
ncit:C7057
.
dgn-gda:DGNe0492d7c956183d51aeff22dc6e791e1
sio:SIO_000628
miriam-gene:4627
,
lld:C0403434
;
a
sio:SIO_001121
.
}
dgn-np:NP476850.RAQfbfFa8gy4kM0tKN_E66wEQfPtORedZdKZ64swl_ZYU130_provenance
{
dgn-np:NP476850.RAQfbfFa8gy4kM0tKN_E66wEQfPtORedZdKZ64swl_ZYU130_assertion
dcterms:description
"[Two African American patients with C1q nephropathy histologically presenting as the collapsing variant of FSGS (collapsing C1q nephropathy) and rapid loss of kidney function were genotyped for polymorphisms in the non-muscle myosin heavy chain 9 gene (MYH9).]. 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:20116156
;
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:NP476850.RAQfbfFa8gy4kM0tKN_E66wEQfPtORedZdKZ64swl_ZYU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:45+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" .
}