@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix orcid: <
http://orcid.org/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP358840.RABkCvNKtt-Hvt4gY_DHIOkZ_0u2t0IGaBCDC04HrIt5w
> .
@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 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:NP358840.RABkCvNKtt-Hvt4gY_DHIOkZ_0u2t0IGaBCDC04HrIt5w130_head
{
this:
np:hasAssertion
dgn-np:NP358840.RABkCvNKtt-Hvt4gY_DHIOkZ_0u2t0IGaBCDC04HrIt5w130_assertion
;
np:hasProvenance
dgn-np:NP358840.RABkCvNKtt-Hvt4gY_DHIOkZ_0u2t0IGaBCDC04HrIt5w130_provenance
;
np:hasPublicationInfo
dgn-np:NP358840.RABkCvNKtt-Hvt4gY_DHIOkZ_0u2t0IGaBCDC04HrIt5w130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP358840.RABkCvNKtt-Hvt4gY_DHIOkZ_0u2t0IGaBCDC04HrIt5w130_assertion
a
np:Assertion
.
dgn-np:NP358840.RABkCvNKtt-Hvt4gY_DHIOkZ_0u2t0IGaBCDC04HrIt5w130_provenance
a
np:Provenance
.
dgn-np:NP358840.RABkCvNKtt-Hvt4gY_DHIOkZ_0u2t0IGaBCDC04HrIt5w130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP358840.RABkCvNKtt-Hvt4gY_DHIOkZ_0u2t0IGaBCDC04HrIt5w130_assertion
{
miriam-gene:8626
a
ncit:C16612
.
lld:C0027627
a
ncit:C7057
.
dgn-gda:DGN907bd262a7d07f390e2c60fd83372d9b
sio:SIO_000628
miriam-gene:8626
,
lld:C0027627
;
a
sio:SIO_001121
.
}
dgn-np:NP358840.RABkCvNKtt-Hvt4gY_DHIOkZ_0u2t0IGaBCDC04HrIt5w130_provenance
{
dgn-np:NP358840.RABkCvNKtt-Hvt4gY_DHIOkZ_0u2t0IGaBCDC04HrIt5w130_assertion
dct:description
"[We review several studies which demonstrate accurate classification of disease phenotypes (e.g., cancer vs. normal), cancer subclasses (e.g., AML vs. ALL, GIST vs. LMS), disease outcomes (e.g., metastasis, survival), and diverse human pathologies assayed through blood-borne leukocytes.]. 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:20218737
;
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:NP358840.RABkCvNKtt-Hvt4gY_DHIOkZ_0u2t0IGaBCDC04HrIt5w130_publicationInfo
{
this:
dct:created
"2014-10-02T12:35:30+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct:subject
sio:SIO_000983
;
prv:usedData
dgn-void:disgenetrdf
;
pav:authoredBy
orcid:0000-0001-5999-6269
,
orcid:0000-0002-7534-7661
,
orcid:0000-0002-9383-528X
,
orcid:0000-0003-0169-8159
,
orcid:0000-0003-1244-7654
;
pav:createdBy
orcid:0000-0003-0169-8159
;
pav:version
"v2.1.0.0" .
dgn-void:disgenetrdf
pav:version
"v2.1.0" .
}