@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8
> .
@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:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_head
{
this:
np:hasAssertion
dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_assertion
;
np:hasProvenance
dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_provenance
;
np:hasPublicationInfo
dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_assertion
a
np:Assertion
.
dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_provenance
a
np:Provenance
.
dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_assertion
{
miriam-gene:5781
a
ncit:C16612
.
lld:C0027819
a
ncit:C7057
.
dgn-gda:DGN7c59ef452207bf2fb43c0730a3603683
sio:SIO_000628
miriam-gene:5781
,
lld:C0027819
;
a
sio:SIO_001121
.
}
dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_provenance
{
dgn-np:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_assertion
dcterms:description
"[Associations between Noonan syndrome and an increased risk of some malignancies, notably leukemia and neuroblastoma, have been reported, and recent data indicate that somatic PTPN11 mutations occur in children with sporadic juvenile myelomonocytic leukemia, myelodysplasic syndrome, B-cell acute lymphoblastic leukemia, and acute myelogenous leukemia (AML).]. 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:15604238
;
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:NP708326.RAqjGLhbWC3RhGheiRvDdyyBR7PJdh3hUAT3a4gjfenP8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:10+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" .
}