@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP281040.RAsHkQKoPK8ZtYv61pNaZyI66tVduOnP4UdVV-PpwPSnc
> .
@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:NP281040.RAsHkQKoPK8ZtYv61pNaZyI66tVduOnP4UdVV-PpwPSnc130_head
{
this:
np:hasAssertion
dgn-np:NP281040.RAsHkQKoPK8ZtYv61pNaZyI66tVduOnP4UdVV-PpwPSnc130_assertion
;
np:hasProvenance
dgn-np:NP281040.RAsHkQKoPK8ZtYv61pNaZyI66tVduOnP4UdVV-PpwPSnc130_provenance
;
np:hasPublicationInfo
dgn-np:NP281040.RAsHkQKoPK8ZtYv61pNaZyI66tVduOnP4UdVV-PpwPSnc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP281040.RAsHkQKoPK8ZtYv61pNaZyI66tVduOnP4UdVV-PpwPSnc130_assertion
a
np:Assertion
.
dgn-np:NP281040.RAsHkQKoPK8ZtYv61pNaZyI66tVduOnP4UdVV-PpwPSnc130_provenance
a
np:Provenance
.
dgn-np:NP281040.RAsHkQKoPK8ZtYv61pNaZyI66tVduOnP4UdVV-PpwPSnc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP281040.RAsHkQKoPK8ZtYv61pNaZyI66tVduOnP4UdVV-PpwPSnc130_assertion
{
miriam-gene:8829
a
ncit:C16612
.
lld:C0334664
a
ncit:C7057
.
dgn-gda:DGN7a8cfcf3a1fc9654a46512ae3ce107a9
sio:SIO_000628
miriam-gene:8829
,
lld:C0334664
;
a
sio:SIO_001121
.
}
dgn-np:NP281040.RAsHkQKoPK8ZtYv61pNaZyI66tVduOnP4UdVV-PpwPSnc130_provenance
{
dgn-np:NP281040.RAsHkQKoPK8ZtYv61pNaZyI66tVduOnP4UdVV-PpwPSnc130_assertion
dcterms:description
"[Most patients with mastocytosis exhibit the D816V point mutation in the tyrosine kinase domain of the transmembrane receptor protein Kit, leading to its constitutive activation in bone marrow or lesional skin tissue.]. 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:16931579
;
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:NP281040.RAsHkQKoPK8ZtYv61pNaZyI66tVduOnP4UdVV-PpwPSnc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:38+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" .
}