@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP280685.RAw7ZKJOdYecGcdpTdyQrYh_FA2ASiawX6DAzbaHeXTGE
> .
@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:NP280685.RAw7ZKJOdYecGcdpTdyQrYh_FA2ASiawX6DAzbaHeXTGE130_head
{
this:
np:hasAssertion
dgn-np:NP280685.RAw7ZKJOdYecGcdpTdyQrYh_FA2ASiawX6DAzbaHeXTGE130_assertion
;
np:hasProvenance
dgn-np:NP280685.RAw7ZKJOdYecGcdpTdyQrYh_FA2ASiawX6DAzbaHeXTGE130_provenance
;
np:hasPublicationInfo
dgn-np:NP280685.RAw7ZKJOdYecGcdpTdyQrYh_FA2ASiawX6DAzbaHeXTGE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP280685.RAw7ZKJOdYecGcdpTdyQrYh_FA2ASiawX6DAzbaHeXTGE130_assertion
a
np:Assertion
.
dgn-np:NP280685.RAw7ZKJOdYecGcdpTdyQrYh_FA2ASiawX6DAzbaHeXTGE130_provenance
a
np:Provenance
.
dgn-np:NP280685.RAw7ZKJOdYecGcdpTdyQrYh_FA2ASiawX6DAzbaHeXTGE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP280685.RAw7ZKJOdYecGcdpTdyQrYh_FA2ASiawX6DAzbaHeXTGE130_assertion
{
miriam-gene:3240
a
ncit:C16612
.
lld:C0010068
a
ncit:C7057
.
dgn-gda:DGN471e6088b6177ea7b95bf721347d51d5
sio:SIO_000628
miriam-gene:3240
,
lld:C0010068
;
a
sio:SIO_001121
.
}
dgn-np:NP280685.RAw7ZKJOdYecGcdpTdyQrYh_FA2ASiawX6DAzbaHeXTGE130_provenance
{
dgn-np:NP280685.RAw7ZKJOdYecGcdpTdyQrYh_FA2ASiawX6DAzbaHeXTGE130_assertion
dcterms:description
"[Haptoglobin (Hp) 2-2 phenotype has been associated with peripheral and coronary artery disease and risk of vascular complications in diabetic patients, but any association of Hp polymorphism with cerebrovascular disease has not been explored so far.]. 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:18691072
;
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:NP280685.RAw7ZKJOdYecGcdpTdyQrYh_FA2ASiawX6DAzbaHeXTGE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:38+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" .
}