@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v3.0.0/void/
> .
dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_head
{
this:
np:hasAssertion
dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_assertion
;
np:hasProvenance
dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_assertion
a
np:Assertion
.
dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_provenance
a
np:Provenance
.
dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_assertion
{
miriam-gene:27115
a
ncit:C16612
.
lld:C0023434
a
ncit:C7057
.
dgn-gda:DGN09b85a9f9622601df7ae0661fcecf986
sio:SIO_000628
miriam-gene:27115
,
lld:C0023434
;
a
sio:SIO_001121
.
}
dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_provenance
{
dgn-np:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_assertion
dcterms:description
"[The low frequency of this 5' untranslated region variant indicates that it does not explain the higher PDE7B expression in patients with CLL but it has the potential to influence other settings that involve a role for PDE7B.]. 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:21796143
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP885953.RAn98075S37pgu4wY9a5l3l1I9vK5yfZVqrxQhyl9ektQ130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:46:39+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:disgenetv3.0rdf
;
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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}