@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP202724.RA3hZT2ZLtNq0HtjFdiSsMtsd9aZUzulc40KgOpEMJPFM
> .
@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:NP202724.RA3hZT2ZLtNq0HtjFdiSsMtsd9aZUzulc40KgOpEMJPFM130_head
{
this:
np:hasAssertion
dgn-np:NP202724.RA3hZT2ZLtNq0HtjFdiSsMtsd9aZUzulc40KgOpEMJPFM130_assertion
;
np:hasProvenance
dgn-np:NP202724.RA3hZT2ZLtNq0HtjFdiSsMtsd9aZUzulc40KgOpEMJPFM130_provenance
;
np:hasPublicationInfo
dgn-np:NP202724.RA3hZT2ZLtNq0HtjFdiSsMtsd9aZUzulc40KgOpEMJPFM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP202724.RA3hZT2ZLtNq0HtjFdiSsMtsd9aZUzulc40KgOpEMJPFM130_assertion
a
np:Assertion
.
dgn-np:NP202724.RA3hZT2ZLtNq0HtjFdiSsMtsd9aZUzulc40KgOpEMJPFM130_provenance
a
np:Provenance
.
dgn-np:NP202724.RA3hZT2ZLtNq0HtjFdiSsMtsd9aZUzulc40KgOpEMJPFM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP202724.RA3hZT2ZLtNq0HtjFdiSsMtsd9aZUzulc40KgOpEMJPFM130_assertion
{
miriam-gene:10855
a
ncit:C16612
.
lld:C1961102
a
ncit:C7057
.
dgn-gda:DGN97dd6b8b72f9e825175b5fd2940a5e52
sio:SIO_000628
miriam-gene:10855
,
lld:C1961102
;
a
sio:SIO_001121
.
}
dgn-np:NP202724.RA3hZT2ZLtNq0HtjFdiSsMtsd9aZUzulc40KgOpEMJPFM130_provenance
{
dgn-np:NP202724.RA3hZT2ZLtNq0HtjFdiSsMtsd9aZUzulc40KgOpEMJPFM130_assertion
dcterms:description
"[These data suggest that certain HPSE gene SNPs may contribute to basal heparanase gene expression and that alterations in this gene are an important determinant in the pathogenesis of ALL, AML and MM.]. 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:17611567
;
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:NP202724.RA3hZT2ZLtNq0HtjFdiSsMtsd9aZUzulc40KgOpEMJPFM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:52+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" .
}