@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP125072.RAdtPk28_0mgLR6FRxu9PQ3Hks2qQhbjHEtR6YQ4UUh00
> .
@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:NP125072.RAdtPk28_0mgLR6FRxu9PQ3Hks2qQhbjHEtR6YQ4UUh00130_head
{
this:
np:hasAssertion
dgn-np:NP125072.RAdtPk28_0mgLR6FRxu9PQ3Hks2qQhbjHEtR6YQ4UUh00130_assertion
;
np:hasProvenance
dgn-np:NP125072.RAdtPk28_0mgLR6FRxu9PQ3Hks2qQhbjHEtR6YQ4UUh00130_provenance
;
np:hasPublicationInfo
dgn-np:NP125072.RAdtPk28_0mgLR6FRxu9PQ3Hks2qQhbjHEtR6YQ4UUh00130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP125072.RAdtPk28_0mgLR6FRxu9PQ3Hks2qQhbjHEtR6YQ4UUh00130_assertion
a
np:Assertion
.
dgn-np:NP125072.RAdtPk28_0mgLR6FRxu9PQ3Hks2qQhbjHEtR6YQ4UUh00130_provenance
a
np:Provenance
.
dgn-np:NP125072.RAdtPk28_0mgLR6FRxu9PQ3Hks2qQhbjHEtR6YQ4UUh00130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP125072.RAdtPk28_0mgLR6FRxu9PQ3Hks2qQhbjHEtR6YQ4UUh00130_assertion
{
miriam-gene:4318
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN5c8c2b4a6b67ac69dd38b855dc0c3b1f
sio:SIO_000628
miriam-gene:4318
,
lld:C0023467
;
a
sio:SIO_001123
.
}
dgn-np:NP125072.RAdtPk28_0mgLR6FRxu9PQ3Hks2qQhbjHEtR6YQ4UUh00130_provenance
{
dgn-np:NP125072.RAdtPk28_0mgLR6FRxu9PQ3Hks2qQhbjHEtR6YQ4UUh00130_assertion
dcterms:description
"[MMP-9 abnormal expression may play a role in the increased vessel density notoriously found in bone marrow of acute myeloid leukemia (AML) patients at diagnosis and thus it may be involved in the leukemogenic process and in myelodysplastic syndrome.]. 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:18081721
;
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:NP125072.RAdtPk28_0mgLR6FRxu9PQ3Hks2qQhbjHEtR6YQ4UUh00130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:05+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" .
}