@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP251106.RAAbY0dQokQWng36t-buHD-C6SmXKDY-e8PNwP8KyVUFs
> .
@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:NP251106.RAAbY0dQokQWng36t-buHD-C6SmXKDY-e8PNwP8KyVUFs130_head
{
this:
np:hasAssertion
dgn-np:NP251106.RAAbY0dQokQWng36t-buHD-C6SmXKDY-e8PNwP8KyVUFs130_assertion
;
np:hasProvenance
dgn-np:NP251106.RAAbY0dQokQWng36t-buHD-C6SmXKDY-e8PNwP8KyVUFs130_provenance
;
np:hasPublicationInfo
dgn-np:NP251106.RAAbY0dQokQWng36t-buHD-C6SmXKDY-e8PNwP8KyVUFs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP251106.RAAbY0dQokQWng36t-buHD-C6SmXKDY-e8PNwP8KyVUFs130_assertion
a
np:Assertion
.
dgn-np:NP251106.RAAbY0dQokQWng36t-buHD-C6SmXKDY-e8PNwP8KyVUFs130_provenance
a
np:Provenance
.
dgn-np:NP251106.RAAbY0dQokQWng36t-buHD-C6SmXKDY-e8PNwP8KyVUFs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP251106.RAAbY0dQokQWng36t-buHD-C6SmXKDY-e8PNwP8KyVUFs130_assertion
{
miriam-gene:3815
a
ncit:C16612
.
lld:C0272203
a
ncit:C7057
.
dgn-gda:DGNa53f7bf6ad116e76d403b1a89d7e3b96
sio:SIO_000628
miriam-gene:3815
,
lld:C0272203
;
a
sio:SIO_001121
.
}
dgn-np:NP251106.RAAbY0dQokQWng36t-buHD-C6SmXKDY-e8PNwP8KyVUFs130_provenance
{
dgn-np:NP251106.RAAbY0dQokQWng36t-buHD-C6SmXKDY-e8PNwP8KyVUFs130_assertion
dcterms:description
"[To our knowledge, this is the first report on the clinical impact of the fraction of KIT D816V mutation positive cells in ISM, which in the present study does not seem to correlate with clinical manifestations of the disease.]. 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:23587333
;
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:NP251106.RAAbY0dQokQWng36t-buHD-C6SmXKDY-e8PNwP8KyVUFs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:20+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" .
}