@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP608899.RAr3U6UZzd0WCyQ2V38NNwT5d2WnxRM7MybJeRbkqWYp8
> .
@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:NP608899.RAr3U6UZzd0WCyQ2V38NNwT5d2WnxRM7MybJeRbkqWYp8130_head
{
this:
np:hasAssertion
dgn-np:NP608899.RAr3U6UZzd0WCyQ2V38NNwT5d2WnxRM7MybJeRbkqWYp8130_assertion
;
np:hasProvenance
dgn-np:NP608899.RAr3U6UZzd0WCyQ2V38NNwT5d2WnxRM7MybJeRbkqWYp8130_provenance
;
np:hasPublicationInfo
dgn-np:NP608899.RAr3U6UZzd0WCyQ2V38NNwT5d2WnxRM7MybJeRbkqWYp8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP608899.RAr3U6UZzd0WCyQ2V38NNwT5d2WnxRM7MybJeRbkqWYp8130_assertion
a
np:Assertion
.
dgn-np:NP608899.RAr3U6UZzd0WCyQ2V38NNwT5d2WnxRM7MybJeRbkqWYp8130_provenance
a
np:Provenance
.
dgn-np:NP608899.RAr3U6UZzd0WCyQ2V38NNwT5d2WnxRM7MybJeRbkqWYp8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP608899.RAr3U6UZzd0WCyQ2V38NNwT5d2WnxRM7MybJeRbkqWYp8130_assertion
{
miriam-gene:3039
a
ncit:C16612
.
lld:C0239161
a
ncit:C7057
.
dgn-gda:DGN5c4ead9d949199154964a01d96cdba96
sio:SIO_000628
miriam-gene:3039
,
lld:C0239161
;
a
sio:SIO_001121
.
}
dgn-np:NP608899.RAr3U6UZzd0WCyQ2V38NNwT5d2WnxRM7MybJeRbkqWYp8130_provenance
{
dgn-np:NP608899.RAr3U6UZzd0WCyQ2V38NNwT5d2WnxRM7MybJeRbkqWYp8130_assertion
dcterms:description
"[Patients with a normal complement of alpha globin genes were 2.2 (1.0, 4.9) times more likely to have benign disease than those with gene deletion, and were less likely to have frequent painful crises, dactylitis, and bone necrosis.]. 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:9120504
;
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:NP608899.RAr3U6UZzd0WCyQ2V38NNwT5d2WnxRM7MybJeRbkqWYp8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:05+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" .
}