@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP806858.RAzL25-EhA_pNMHjlxomF7a_mqkMKaJydOCgcVMDDWiRQ
> .
@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:NP806858.RAzL25-EhA_pNMHjlxomF7a_mqkMKaJydOCgcVMDDWiRQ130_head
{
this:
np:hasAssertion
dgn-np:NP806858.RAzL25-EhA_pNMHjlxomF7a_mqkMKaJydOCgcVMDDWiRQ130_assertion
;
np:hasProvenance
dgn-np:NP806858.RAzL25-EhA_pNMHjlxomF7a_mqkMKaJydOCgcVMDDWiRQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP806858.RAzL25-EhA_pNMHjlxomF7a_mqkMKaJydOCgcVMDDWiRQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP806858.RAzL25-EhA_pNMHjlxomF7a_mqkMKaJydOCgcVMDDWiRQ130_assertion
a
np:Assertion
.
dgn-np:NP806858.RAzL25-EhA_pNMHjlxomF7a_mqkMKaJydOCgcVMDDWiRQ130_provenance
a
np:Provenance
.
dgn-np:NP806858.RAzL25-EhA_pNMHjlxomF7a_mqkMKaJydOCgcVMDDWiRQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP806858.RAzL25-EhA_pNMHjlxomF7a_mqkMKaJydOCgcVMDDWiRQ130_assertion
{
miriam-gene:1822
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN76e9e21ac33dfdb681f90c03ccfd4018
sio:SIO_000628
miriam-gene:1822
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP806858.RAzL25-EhA_pNMHjlxomF7a_mqkMKaJydOCgcVMDDWiRQ130_provenance
{
dgn-np:NP806858.RAzL25-EhA_pNMHjlxomF7a_mqkMKaJydOCgcVMDDWiRQ130_assertion
dcterms:description
"[In addition, the difference in the ability of AML LTC-IC and NOD/SL-IC to survive ex vivo suggests that these assays may detect different populations of cells or that changes are induced in vitro in primitive cells which can only be detected in the mouse assay.]. 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:10560908
;
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:NP806858.RAzL25-EhA_pNMHjlxomF7a_mqkMKaJydOCgcVMDDWiRQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:15+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" .
}