@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP654235.RAOntuOw2e_Vq7ohDJpH0YYk0uJPOvrdJ6idsT8m8PuCU
> .
@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:NP654235.RAOntuOw2e_Vq7ohDJpH0YYk0uJPOvrdJ6idsT8m8PuCU130_head
{
this:
np:hasAssertion
dgn-np:NP654235.RAOntuOw2e_Vq7ohDJpH0YYk0uJPOvrdJ6idsT8m8PuCU130_assertion
;
np:hasProvenance
dgn-np:NP654235.RAOntuOw2e_Vq7ohDJpH0YYk0uJPOvrdJ6idsT8m8PuCU130_provenance
;
np:hasPublicationInfo
dgn-np:NP654235.RAOntuOw2e_Vq7ohDJpH0YYk0uJPOvrdJ6idsT8m8PuCU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP654235.RAOntuOw2e_Vq7ohDJpH0YYk0uJPOvrdJ6idsT8m8PuCU130_assertion
a
np:Assertion
.
dgn-np:NP654235.RAOntuOw2e_Vq7ohDJpH0YYk0uJPOvrdJ6idsT8m8PuCU130_provenance
a
np:Provenance
.
dgn-np:NP654235.RAOntuOw2e_Vq7ohDJpH0YYk0uJPOvrdJ6idsT8m8PuCU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP654235.RAOntuOw2e_Vq7ohDJpH0YYk0uJPOvrdJ6idsT8m8PuCU130_assertion
{
miriam-gene:2260
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGNc9c0430c826646c99e3d9fe1988218f6
sio:SIO_000628
miriam-gene:2260
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP654235.RAOntuOw2e_Vq7ohDJpH0YYk0uJPOvrdJ6idsT8m8PuCU130_provenance
{
dgn-np:NP654235.RAOntuOw2e_Vq7ohDJpH0YYk0uJPOvrdJ6idsT8m8PuCU130_assertion
dcterms:description
"[The fourth edition of the WHO classification provides a framework to incorporate those neoplasms in which a genetic abnormality is a major defining criterion of the disease, such as those associated with eosinophilia and abnormalities of PDGFRA, PDGFRB, and FGFR1, as well as for those in which no specific genetic defect has yet been discovered and which remain clinically and pathologically defined.]. 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:22160042
;
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:NP654235.RAOntuOw2e_Vq7ohDJpH0YYk0uJPOvrdJ6idsT8m8PuCU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:34+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" .
}