@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP136083.RAr1u8ZfixDqtZwVGAv7ipH9dyxwclmsUV3E9adFiEHyA
> .
@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:NP136083.RAr1u8ZfixDqtZwVGAv7ipH9dyxwclmsUV3E9adFiEHyA130_head
{
this:
np:hasAssertion
dgn-np:NP136083.RAr1u8ZfixDqtZwVGAv7ipH9dyxwclmsUV3E9adFiEHyA130_assertion
;
np:hasProvenance
dgn-np:NP136083.RAr1u8ZfixDqtZwVGAv7ipH9dyxwclmsUV3E9adFiEHyA130_provenance
;
np:hasPublicationInfo
dgn-np:NP136083.RAr1u8ZfixDqtZwVGAv7ipH9dyxwclmsUV3E9adFiEHyA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP136083.RAr1u8ZfixDqtZwVGAv7ipH9dyxwclmsUV3E9adFiEHyA130_assertion
a
np:Assertion
.
dgn-np:NP136083.RAr1u8ZfixDqtZwVGAv7ipH9dyxwclmsUV3E9adFiEHyA130_provenance
a
np:Provenance
.
dgn-np:NP136083.RAr1u8ZfixDqtZwVGAv7ipH9dyxwclmsUV3E9adFiEHyA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP136083.RAr1u8ZfixDqtZwVGAv7ipH9dyxwclmsUV3E9adFiEHyA130_assertion
{
miriam-gene:3119
a
ncit:C16612
.
lld:C0002895
a
ncit:C7057
.
dgn-gda:DGNd335713a5cff7d711ac19d76d09199ee
sio:SIO_000628
miriam-gene:3119
,
lld:C0002895
;
a
sio:SIO_001122
.
}
dgn-np:NP136083.RAr1u8ZfixDqtZwVGAv7ipH9dyxwclmsUV3E9adFiEHyA130_provenance
{
dgn-np:NP136083.RAr1u8ZfixDqtZwVGAv7ipH9dyxwclmsUV3E9adFiEHyA130_assertion
dcterms:description
"[results show that specific HLA haplotypes influence sickle cell anemia (SCA) osteomyelitis risk and that specific HLA types may serve as markers for identifying SCA patients at high risk for osteomyelitis ]. 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:18312480
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP136083.RAr1u8ZfixDqtZwVGAv7ipH9dyxwclmsUV3E9adFiEHyA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:11+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" .
}