@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP881204.RAEI0UtZmACgZhk4nUJ0i0Wy80Hzxh7abSoUxauLkvcHE
> .
@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:NP881204.RAEI0UtZmACgZhk4nUJ0i0Wy80Hzxh7abSoUxauLkvcHE130_head
{
this:
np:hasAssertion
dgn-np:NP881204.RAEI0UtZmACgZhk4nUJ0i0Wy80Hzxh7abSoUxauLkvcHE130_assertion
;
np:hasProvenance
dgn-np:NP881204.RAEI0UtZmACgZhk4nUJ0i0Wy80Hzxh7abSoUxauLkvcHE130_provenance
;
np:hasPublicationInfo
dgn-np:NP881204.RAEI0UtZmACgZhk4nUJ0i0Wy80Hzxh7abSoUxauLkvcHE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP881204.RAEI0UtZmACgZhk4nUJ0i0Wy80Hzxh7abSoUxauLkvcHE130_assertion
a
np:Assertion
.
dgn-np:NP881204.RAEI0UtZmACgZhk4nUJ0i0Wy80Hzxh7abSoUxauLkvcHE130_provenance
a
np:Provenance
.
dgn-np:NP881204.RAEI0UtZmACgZhk4nUJ0i0Wy80Hzxh7abSoUxauLkvcHE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP881204.RAEI0UtZmACgZhk4nUJ0i0Wy80Hzxh7abSoUxauLkvcHE130_assertion
{
miriam-gene:2131
a
ncit:C16612
.
lld:C0002874
a
ncit:C7057
.
dgn-gda:DGN36fd618037749e23c8e5b27b1805e720
sio:SIO_000628
miriam-gene:2131
,
lld:C0002874
;
a
sio:SIO_001121
.
}
dgn-np:NP881204.RAEI0UtZmACgZhk4nUJ0i0Wy80Hzxh7abSoUxauLkvcHE130_provenance
{
dgn-np:NP881204.RAEI0UtZmACgZhk4nUJ0i0Wy80Hzxh7abSoUxauLkvcHE130_assertion
dcterms:description
"[We investigated the prevalence of TTV DNA in human hematopoietic cells, based on 84 mononuclear cell samples obtained from the bone marrow or lymph nodes of patients with hematopoietic malignancies including leukemia, malignant lymphoma and aplastic anemia.]. 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:10830749
;
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:NP881204.RAEI0UtZmACgZhk4nUJ0i0Wy80Hzxh7abSoUxauLkvcHE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:58+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" .
}