@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE
> .
@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 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:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_head
{
this:
np:hasAssertion
dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_assertion
;
np:hasProvenance
dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_provenance
;
np:hasPublicationInfo
dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_assertion
a
np:Assertion
.
dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_provenance
a
np:Provenance
.
dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_assertion
{
miriam-gene:302
a
ncit:C16612
.
lld:C0029445
a
ncit:C7057
.
dgn-gda:DGN0270070fd20e125e5350cb266d0f1ad9
sio:SIO_000628
miriam-gene:302
,
lld:C0029445
;
a
sio:SIO_001122
.
}
dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_provenance
{
dgn-np:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_assertion
dct:description
"[These genes are important in bone morphology, metabolism and vascular disease. Our results may provide insight into the pathogenesis of osteonecrosis in sickle cell disease, help identify individuals who are at high risk for osteonecrosis, and thus allow earlier and more effective therapeutic intervention.]. 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:15784727
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP59551.RAwxZNxSrBj92zL1lclCx3XvqAz-_d0rDcTwO5eDHc-jE130_publicationInfo
{
this:
dct:created
"2014-10-02T12:32:28+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}