@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP749541.RAG0MZgonYBUXm86zUB9o1-IiUcfGx9OCCqTqF5FEkVak
> .
@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:NP749541.RAG0MZgonYBUXm86zUB9o1-IiUcfGx9OCCqTqF5FEkVak130_head
{
this:
np:hasAssertion
dgn-np:NP749541.RAG0MZgonYBUXm86zUB9o1-IiUcfGx9OCCqTqF5FEkVak130_assertion
;
np:hasProvenance
dgn-np:NP749541.RAG0MZgonYBUXm86zUB9o1-IiUcfGx9OCCqTqF5FEkVak130_provenance
;
np:hasPublicationInfo
dgn-np:NP749541.RAG0MZgonYBUXm86zUB9o1-IiUcfGx9OCCqTqF5FEkVak130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP749541.RAG0MZgonYBUXm86zUB9o1-IiUcfGx9OCCqTqF5FEkVak130_assertion
a
np:Assertion
.
dgn-np:NP749541.RAG0MZgonYBUXm86zUB9o1-IiUcfGx9OCCqTqF5FEkVak130_provenance
a
np:Provenance
.
dgn-np:NP749541.RAG0MZgonYBUXm86zUB9o1-IiUcfGx9OCCqTqF5FEkVak130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP749541.RAG0MZgonYBUXm86zUB9o1-IiUcfGx9OCCqTqF5FEkVak130_assertion
{
miriam-gene:728358
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGN5614dece0edc5d2eb959e3f767229471
sio:SIO_000628
miriam-gene:728358
,
lld:C0023434
;
a
sio:SIO_001121
.
}
dgn-np:NP749541.RAG0MZgonYBUXm86zUB9o1-IiUcfGx9OCCqTqF5FEkVak130_provenance
{
dgn-np:NP749541.RAG0MZgonYBUXm86zUB9o1-IiUcfGx9OCCqTqF5FEkVak130_assertion
dcterms:description
"[The phenotype HP1 was found to have an increased incidence in the total patient group due to an increased incidence in those with AML, ALL and CML compared with controls, but not in those with CLL.]. 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:3397067
;
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:NP749541.RAG0MZgonYBUXm86zUB9o1-IiUcfGx9OCCqTqF5FEkVak130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:34+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" .
}