@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP265513.RApBPwZqC3VgYNQGIFJZUmkaYt8zxU0BWGUqgNsjdAXYI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP265513.RApBPwZqC3VgYNQGIFJZUmkaYt8zxU0BWGUqgNsjdAXYI130_head
{
this:
np:hasAssertion
dgn-np:NP265513.RApBPwZqC3VgYNQGIFJZUmkaYt8zxU0BWGUqgNsjdAXYI130_assertion
;
np:hasProvenance
dgn-np:NP265513.RApBPwZqC3VgYNQGIFJZUmkaYt8zxU0BWGUqgNsjdAXYI130_provenance
;
np:hasPublicationInfo
dgn-np:NP265513.RApBPwZqC3VgYNQGIFJZUmkaYt8zxU0BWGUqgNsjdAXYI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP265513.RApBPwZqC3VgYNQGIFJZUmkaYt8zxU0BWGUqgNsjdAXYI130_assertion
a
np:Assertion
.
dgn-np:NP265513.RApBPwZqC3VgYNQGIFJZUmkaYt8zxU0BWGUqgNsjdAXYI130_provenance
a
np:Provenance
.
dgn-np:NP265513.RApBPwZqC3VgYNQGIFJZUmkaYt8zxU0BWGUqgNsjdAXYI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP265513.RApBPwZqC3VgYNQGIFJZUmkaYt8zxU0BWGUqgNsjdAXYI130_assertion
{
miriam-gene:4524
a
ncit:C16612
.
lld:C0598608
a
ncit:C7057
.
dgn-gda:DGN83dc693cf6716879e2ecce16707686b5
sio:SIO_000628
miriam-gene:4524
,
lld:C0598608
;
a
sio:SIO_001122
.
}
dgn-np:NP265513.RApBPwZqC3VgYNQGIFJZUmkaYt8zxU0BWGUqgNsjdAXYI130_provenance
{
dgn-np:NP265513.RApBPwZqC3VgYNQGIFJZUmkaYt8zxU0BWGUqgNsjdAXYI130_assertion
dcterms:description
"[To determine the role of hyperhomocysteinemia in the pathogenesis of stroke in children with sickle cell disease (SCD), Hcy levels and C677T MTHFR genotype were determined in 40 patients homozygous for hemoglobin SS and compared with 197 healthy children.]. 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:10524453
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP265513.RApBPwZqC3VgYNQGIFJZUmkaYt8zxU0BWGUqgNsjdAXYI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:46+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}