@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg
> .
@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:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_head
{
this:
np:hasAssertion
dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_assertion
;
np:hasProvenance
dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_provenance
;
np:hasPublicationInfo
dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_assertion
a
np:Assertion
.
dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_provenance
a
np:Provenance
.
dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_assertion
{
miriam-gene:3240
a
ncit:C16612
.
lld:C0023343
a
ncit:C7057
.
dgn-gda:DGN95400644ce71f981daacf6ed157eb843
sio:SIO_000628
miriam-gene:3240
,
lld:C0023343
;
a
sio:SIO_001121
.
}
dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_provenance
{
dgn-np:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_assertion
dcterms:description
"[Thus, although this genetic marker did not correlate with the occurrence of the variety of disease, it is possible that leprosy caused inhibition of haptoglobin synthesis and therefore an apparent increased frequency of the 0-0 phenotype.]. 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:7193656
;
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:NP683143.RAl36fsD6mkMM1IHCg_X-f1gYaWt9PvnYZiHI6GKKipcg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:55+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" .
}