@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q
> .
@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:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_head
{
this:
np:hasAssertion
dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_assertion
;
np:hasProvenance
dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_assertion
a
np:Assertion
.
dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_provenance
a
np:Provenance
.
dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_assertion
{
miriam-gene:4893
a
ncit:C16612
.
lld:C0023473
a
ncit:C7057
.
dgn-gda:DGN596241fef5145ddec86be478d55b5ea4
sio:SIO_000628
miriam-gene:4893
,
lld:C0023473
;
a
sio:SIO_001121
.
}
dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_provenance
{
dgn-np:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_assertion
dcterms:description
"[Using the polymerase chain reaction-single strand conformation polymorphism method and direct sequencing, 12 acute myeloid leukemia (AML) cell lines and 108 fresh childhood myeloid tumor specimens, including 67 AML, 29 myelodysplastic syndrome (MDS), and 12 juvenile chronic myelocytic leukemia (JCML) were examined for mutation in H-, K-, and N-RAS genes.]. 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:9379676
;
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:NP660685.RAYzPEMk1caG2Z5Sd-SZ3HxvJ9CgDIPeSQSVDn7D0zj8Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:39+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" .
}