@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP210683.RA_6kVrp_4eF3Ee0BJYelsE_9JlzntTU4KjfRoVOK0j1k
> .
@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:NP210683.RA_6kVrp_4eF3Ee0BJYelsE_9JlzntTU4KjfRoVOK0j1k130_head
{
this:
np:hasAssertion
dgn-np:NP210683.RA_6kVrp_4eF3Ee0BJYelsE_9JlzntTU4KjfRoVOK0j1k130_assertion
;
np:hasProvenance
dgn-np:NP210683.RA_6kVrp_4eF3Ee0BJYelsE_9JlzntTU4KjfRoVOK0j1k130_provenance
;
np:hasPublicationInfo
dgn-np:NP210683.RA_6kVrp_4eF3Ee0BJYelsE_9JlzntTU4KjfRoVOK0j1k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP210683.RA_6kVrp_4eF3Ee0BJYelsE_9JlzntTU4KjfRoVOK0j1k130_assertion
a
np:Assertion
.
dgn-np:NP210683.RA_6kVrp_4eF3Ee0BJYelsE_9JlzntTU4KjfRoVOK0j1k130_provenance
a
np:Provenance
.
dgn-np:NP210683.RA_6kVrp_4eF3Ee0BJYelsE_9JlzntTU4KjfRoVOK0j1k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP210683.RA_6kVrp_4eF3Ee0BJYelsE_9JlzntTU4KjfRoVOK0j1k130_assertion
{
miriam-gene:1437
a
ncit:C16612
.
lld:C0349639
a
ncit:C7057
.
dgn-gda:DGNe992576d63f72088e7eed8ce49bfc606
sio:SIO_000628
miriam-gene:1437
,
lld:C0349639
;
a
sio:SIO_001121
.
}
dgn-np:NP210683.RA_6kVrp_4eF3Ee0BJYelsE_9JlzntTU4KjfRoVOK0j1k130_provenance
{
dgn-np:NP210683.RA_6kVrp_4eF3Ee0BJYelsE_9JlzntTU4KjfRoVOK0j1k130_assertion
dcterms:description
"[Mutations in SHP-2 phosphatase that cause hyperactivation of its catalytic activity have been identified in human leukemias, particularly juvenile myelomonocytic leukemia, which is characterized by hypersensitivity of myeloid progenitor cells to granulocyte macrophage colony-stimulating factor and interleukin (IL)-3.]. 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:16371368
;
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:NP210683.RA_6kVrp_4eF3Ee0BJYelsE_9JlzntTU4KjfRoVOK0j1k130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:56+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" .
}