@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP59097.RAgvWZiaXnPapZEjpzc0nDL6UPOnx3J9Chf5o1JeDHCOQ
> .
@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:NP59097.RAgvWZiaXnPapZEjpzc0nDL6UPOnx3J9Chf5o1JeDHCOQ130_head
{
this:
np:hasAssertion
dgn-np:NP59097.RAgvWZiaXnPapZEjpzc0nDL6UPOnx3J9Chf5o1JeDHCOQ130_assertion
;
np:hasProvenance
dgn-np:NP59097.RAgvWZiaXnPapZEjpzc0nDL6UPOnx3J9Chf5o1JeDHCOQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP59097.RAgvWZiaXnPapZEjpzc0nDL6UPOnx3J9Chf5o1JeDHCOQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP59097.RAgvWZiaXnPapZEjpzc0nDL6UPOnx3J9Chf5o1JeDHCOQ130_assertion
a
np:Assertion
.
dgn-np:NP59097.RAgvWZiaXnPapZEjpzc0nDL6UPOnx3J9Chf5o1JeDHCOQ130_provenance
a
np:Provenance
.
dgn-np:NP59097.RAgvWZiaXnPapZEjpzc0nDL6UPOnx3J9Chf5o1JeDHCOQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP59097.RAgvWZiaXnPapZEjpzc0nDL6UPOnx3J9Chf5o1JeDHCOQ130_assertion
{
miriam-gene:7421
a
ncit:C16612
.
lld:C0029445
a
ncit:C7057
.
dgn-gda:DGNae4173f4172b845698e2164e28d90303
sio:SIO_000628
miriam-gene:7421
,
lld:C0029445
;
a
sio:SIO_001122
.
}
dgn-np:NP59097.RAgvWZiaXnPapZEjpzc0nDL6UPOnx3J9Chf5o1JeDHCOQ130_provenance
{
dgn-np:NP59097.RAgvWZiaXnPapZEjpzc0nDL6UPOnx3J9Chf5o1JeDHCOQ130_assertion
dcterms:description
"[ Because folate-related and vitamin D-receptor genetic variants have been associated with bone and vasculature morbidity, these pharmacogenetic associations likely reflect the interaction of antileukemic medications with germline sensitivity to drug actions, and might identify ALL patients at highest risk to develop osteonecrosis.]. 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:15459215
;
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:NP59097.RAgvWZiaXnPapZEjpzc0nDL6UPOnx3J9Chf5o1JeDHCOQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:27+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" .
}