@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP721449.RASpesPgbklYEGfFO827ulr_MhJJ0-edopjcL1Tf2o5Mc
> .
@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:NP721449.RASpesPgbklYEGfFO827ulr_MhJJ0-edopjcL1Tf2o5Mc130_head
{
this:
np:hasAssertion
dgn-np:NP721449.RASpesPgbklYEGfFO827ulr_MhJJ0-edopjcL1Tf2o5Mc130_assertion
;
np:hasProvenance
dgn-np:NP721449.RASpesPgbklYEGfFO827ulr_MhJJ0-edopjcL1Tf2o5Mc130_provenance
;
np:hasPublicationInfo
dgn-np:NP721449.RASpesPgbklYEGfFO827ulr_MhJJ0-edopjcL1Tf2o5Mc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP721449.RASpesPgbklYEGfFO827ulr_MhJJ0-edopjcL1Tf2o5Mc130_assertion
a
np:Assertion
.
dgn-np:NP721449.RASpesPgbklYEGfFO827ulr_MhJJ0-edopjcL1Tf2o5Mc130_provenance
a
np:Provenance
.
dgn-np:NP721449.RASpesPgbklYEGfFO827ulr_MhJJ0-edopjcL1Tf2o5Mc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP721449.RASpesPgbklYEGfFO827ulr_MhJJ0-edopjcL1Tf2o5Mc130_assertion
{
miriam-gene:3098
a
ncit:C16612
.
lld:C0002871
a
ncit:C7057
.
dgn-gda:DGN403c894ef2a673ca9657c85edff902b1
sio:SIO_000628
miriam-gene:3098
,
lld:C0002871
;
a
sio:SIO_001121
.
}
dgn-np:NP721449.RASpesPgbklYEGfFO827ulr_MhJJ0-edopjcL1Tf2o5Mc130_provenance
{
dgn-np:NP721449.RASpesPgbklYEGfFO827ulr_MhJJ0-edopjcL1Tf2o5Mc130_assertion
dcterms:description
"[Since HK1 rs7072268 is associated with reduced hemoglobin levels and favors anemia, we propose that HK1 may influence A1C levels through its anemic effect or its effect on glucose metabolism in RBCs.]. 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:19651813
;
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:NP721449.RASpesPgbklYEGfFO827ulr_MhJJ0-edopjcL1Tf2o5Mc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:18+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" .
}