@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP172691.RAJ_UgJBoD6ZZPglcZMJPnVxB6jAPksCPY4xkxuR9a3xo
> .
@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:NP172691.RAJ_UgJBoD6ZZPglcZMJPnVxB6jAPksCPY4xkxuR9a3xo130_head
{
this:
np:hasAssertion
dgn-np:NP172691.RAJ_UgJBoD6ZZPglcZMJPnVxB6jAPksCPY4xkxuR9a3xo130_assertion
;
np:hasProvenance
dgn-np:NP172691.RAJ_UgJBoD6ZZPglcZMJPnVxB6jAPksCPY4xkxuR9a3xo130_provenance
;
np:hasPublicationInfo
dgn-np:NP172691.RAJ_UgJBoD6ZZPglcZMJPnVxB6jAPksCPY4xkxuR9a3xo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP172691.RAJ_UgJBoD6ZZPglcZMJPnVxB6jAPksCPY4xkxuR9a3xo130_assertion
a
np:Assertion
.
dgn-np:NP172691.RAJ_UgJBoD6ZZPglcZMJPnVxB6jAPksCPY4xkxuR9a3xo130_provenance
a
np:Provenance
.
dgn-np:NP172691.RAJ_UgJBoD6ZZPglcZMJPnVxB6jAPksCPY4xkxuR9a3xo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP172691.RAJ_UgJBoD6ZZPglcZMJPnVxB6jAPksCPY4xkxuR9a3xo130_assertion
{
miriam-gene:3815
a
ncit:C16612
.
lld:C0024899
a
ncit:C7057
.
dgn-gda:DGNce99e0deb4c684df5df278692adddbf5
sio:SIO_000628
miriam-gene:3815
,
lld:C0024899
;
a
sio:SIO_001121
.
}
dgn-np:NP172691.RAJ_UgJBoD6ZZPglcZMJPnVxB6jAPksCPY4xkxuR9a3xo130_provenance
{
dgn-np:NP172691.RAJ_UgJBoD6ZZPglcZMJPnVxB6jAPksCPY4xkxuR9a3xo130_assertion
dcterms:description
"[Point mutations of the C-KIT gene, previously implicated in the genesis of mastocytosis, were discovered not only in the bone marrow and the peripheral blood of the patient, but also in the tissue of the previously diagnosed germ cell tumor as well.]. 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:17551405
;
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:NP172691.RAJ_UgJBoD6ZZPglcZMJPnVxB6jAPksCPY4xkxuR9a3xo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:33+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" .
}