@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP255337.RAlKhkOK3_94e400k6uu6wt0S2g-HcPX-AnhWt_WV6T4c
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP255337.RAlKhkOK3_94e400k6uu6wt0S2g-HcPX-AnhWt_WV6T4c130_assertion
;
np:hasProvenance
dgn-np:NP255337.RAlKhkOK3_94e400k6uu6wt0S2g-HcPX-AnhWt_WV6T4c130_provenance
;
np:hasPublicationInfo
dgn-np:NP255337.RAlKhkOK3_94e400k6uu6wt0S2g-HcPX-AnhWt_WV6T4c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP255337.RAlKhkOK3_94e400k6uu6wt0S2g-HcPX-AnhWt_WV6T4c130_assertion
a
np:Assertion
.
dgn-np:NP255337.RAlKhkOK3_94e400k6uu6wt0S2g-HcPX-AnhWt_WV6T4c130_provenance
a
np:Provenance
.
dgn-np:NP255337.RAlKhkOK3_94e400k6uu6wt0S2g-HcPX-AnhWt_WV6T4c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP255337.RAlKhkOK3_94e400k6uu6wt0S2g-HcPX-AnhWt_WV6T4c130_assertion
{
miriam-gene:4627
a
ncit:C16612
.
lld:C0022661
a
ncit:C7057
.
dgn-gda:DGN74747eff061f76d45035df779f8383fa
sio:SIO_000628
miriam-gene:4627
,
lld:C0022661
;
a
sio:SIO_001121
.
}
dgn-np:NP255337.RAlKhkOK3_94e400k6uu6wt0S2g-HcPX-AnhWt_WV6T4c130_provenance
{
dgn-np:NP255337.RAlKhkOK3_94e400k6uu6wt0S2g-HcPX-AnhWt_WV6T4c130_assertion
dcterms:description
"[These findings strengthen the contention that a sequence variant of MYH9, common in populations with varying degrees of African ancestry admixture, and in strong linkage disequilibrium with the associated SNPs and haplotypes reported herein, strongly predisposes to non-diabetic ESKD.]. 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:20144966
;
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:NP255337.RAlKhkOK3_94e400k6uu6wt0S2g-HcPX-AnhWt_WV6T4c130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:22+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" .
}