@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP449263.RAer2McAiZgAjvg6s_APEhr0fkMiuJ70xFo2s83Dxm7Sw
> .
@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:NP449263.RAer2McAiZgAjvg6s_APEhr0fkMiuJ70xFo2s83Dxm7Sw130_head
{
this:
np:hasAssertion
dgn-np:NP449263.RAer2McAiZgAjvg6s_APEhr0fkMiuJ70xFo2s83Dxm7Sw130_assertion
;
np:hasProvenance
dgn-np:NP449263.RAer2McAiZgAjvg6s_APEhr0fkMiuJ70xFo2s83Dxm7Sw130_provenance
;
np:hasPublicationInfo
dgn-np:NP449263.RAer2McAiZgAjvg6s_APEhr0fkMiuJ70xFo2s83Dxm7Sw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP449263.RAer2McAiZgAjvg6s_APEhr0fkMiuJ70xFo2s83Dxm7Sw130_assertion
a
np:Assertion
.
dgn-np:NP449263.RAer2McAiZgAjvg6s_APEhr0fkMiuJ70xFo2s83Dxm7Sw130_provenance
a
np:Provenance
.
dgn-np:NP449263.RAer2McAiZgAjvg6s_APEhr0fkMiuJ70xFo2s83Dxm7Sw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP449263.RAer2McAiZgAjvg6s_APEhr0fkMiuJ70xFo2s83Dxm7Sw130_assertion
{
miriam-gene:5156
a
ncit:C16612
.
lld:C0027651
a
ncit:C7057
.
dgn-gda:DGN27c18fd9dfcef64f1e238670bfb63328
sio:SIO_000628
miriam-gene:5156
,
lld:C0027651
;
a
sio:SIO_001121
.
}
dgn-np:NP449263.RAer2McAiZgAjvg6s_APEhr0fkMiuJ70xFo2s83Dxm7Sw130_provenance
{
dgn-np:NP449263.RAer2McAiZgAjvg6s_APEhr0fkMiuJ70xFo2s83Dxm7Sw130_assertion
dcterms:description
"[The low frequency of clinical resistance to PDGFR inhibitors in myeloid neoplasms with abnormalities of PDGFRA might be related to the limited repertoire of possible PDGFRA kinase domain mutations in vitro.]. 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:20972453
;
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:NP449263.RAer2McAiZgAjvg6s_APEhr0fkMiuJ70xFo2s83Dxm7Sw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:28+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" .
}