@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP893228.RAzDy8PuJcaEz1KQ4C1UZ4EE0RoBXIYVUm4g-bTrZKa-A
> .
@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:NP893228.RAzDy8PuJcaEz1KQ4C1UZ4EE0RoBXIYVUm4g-bTrZKa-A130_head
{
this:
np:hasAssertion
dgn-np:NP893228.RAzDy8PuJcaEz1KQ4C1UZ4EE0RoBXIYVUm4g-bTrZKa-A130_assertion
;
np:hasProvenance
dgn-np:NP893228.RAzDy8PuJcaEz1KQ4C1UZ4EE0RoBXIYVUm4g-bTrZKa-A130_provenance
;
np:hasPublicationInfo
dgn-np:NP893228.RAzDy8PuJcaEz1KQ4C1UZ4EE0RoBXIYVUm4g-bTrZKa-A130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP893228.RAzDy8PuJcaEz1KQ4C1UZ4EE0RoBXIYVUm4g-bTrZKa-A130_assertion
a
np:Assertion
.
dgn-np:NP893228.RAzDy8PuJcaEz1KQ4C1UZ4EE0RoBXIYVUm4g-bTrZKa-A130_provenance
a
np:Provenance
.
dgn-np:NP893228.RAzDy8PuJcaEz1KQ4C1UZ4EE0RoBXIYVUm4g-bTrZKa-A130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP893228.RAzDy8PuJcaEz1KQ4C1UZ4EE0RoBXIYVUm4g-bTrZKa-A130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0349632
a
ncit:C7057
.
dgn-gda:DGNe2ccd530d0b4bbfffe3cac24567dbdef
sio:SIO_000628
miriam-gene:7157
,
lld:C0349632
;
a
sio:SIO_001121
.
}
dgn-np:NP893228.RAzDy8PuJcaEz1KQ4C1UZ4EE0RoBXIYVUm4g-bTrZKa-A130_provenance
{
dgn-np:NP893228.RAzDy8PuJcaEz1KQ4C1UZ4EE0RoBXIYVUm4g-bTrZKa-A130_assertion
dcterms:description
"[CONCLUSIONS; In spite of a diffuse pattern of splenic infiltration, cutaneous involvement and p53 alterations, these cases have findings that overlap with those corresponding to classic SMZL (symptomatology, morphology of bone marrow, lymph nodes, peripheral blood involvement, and immunophenotype).]. 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:11903595
;
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:NP893228.RAzDy8PuJcaEz1KQ4C1UZ4EE0RoBXIYVUm4g-bTrZKa-A130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:09+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" .
}