@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP816117.RAeWGE32dcZXRjaGXMOIHzP85C9Vsf5XBlhiOLz7_tP90
> .
@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:NP816117.RAeWGE32dcZXRjaGXMOIHzP85C9Vsf5XBlhiOLz7_tP90130_head
{
this:
np:hasAssertion
dgn-np:NP816117.RAeWGE32dcZXRjaGXMOIHzP85C9Vsf5XBlhiOLz7_tP90130_assertion
;
np:hasProvenance
dgn-np:NP816117.RAeWGE32dcZXRjaGXMOIHzP85C9Vsf5XBlhiOLz7_tP90130_provenance
;
np:hasPublicationInfo
dgn-np:NP816117.RAeWGE32dcZXRjaGXMOIHzP85C9Vsf5XBlhiOLz7_tP90130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP816117.RAeWGE32dcZXRjaGXMOIHzP85C9Vsf5XBlhiOLz7_tP90130_assertion
a
np:Assertion
.
dgn-np:NP816117.RAeWGE32dcZXRjaGXMOIHzP85C9Vsf5XBlhiOLz7_tP90130_provenance
a
np:Provenance
.
dgn-np:NP816117.RAeWGE32dcZXRjaGXMOIHzP85C9Vsf5XBlhiOLz7_tP90130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP816117.RAeWGE32dcZXRjaGXMOIHzP85C9Vsf5XBlhiOLz7_tP90130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0002871
a
ncit:C7057
.
dgn-gda:DGN1f168408ae353c72aab3db38c6fba01b
sio:SIO_000628
miriam-gene:7421
,
lld:C0002871
;
a
sio:SIO_001121
.
}
dgn-np:NP816117.RAeWGE32dcZXRjaGXMOIHzP85C9Vsf5XBlhiOLz7_tP90130_provenance
{
dgn-np:NP816117.RAeWGE32dcZXRjaGXMOIHzP85C9Vsf5XBlhiOLz7_tP90130_assertion
dcterms:description
"[In addition to well-known factors responsible for both anemia and inadequate response to erythropoietin (EPO), we examined the contribution of the VDR genotype to hematocrit (Hct), hemoglobin (Hb) level, total weekly dose of EPO, and EPO-Hb ratio as an index of patient EPO need.]. 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:12324918
;
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:NP816117.RAeWGE32dcZXRjaGXMOIHzP85C9Vsf5XBlhiOLz7_tP90130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:20+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" .
}