@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys
> .
@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:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_head
{
this:
np:hasAssertion
dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_assertion
;
np:hasProvenance
dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_provenance
;
np:hasPublicationInfo
dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_assertion
a
np:Assertion
.
dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_provenance
a
np:Provenance
.
dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_assertion
{
miriam-gene:1950
a
ncit:C16612
.
lld:C0026986
a
ncit:C7057
.
dgn-gda:DGN4b2b73923d86fa19c251db023ae38ccb
sio:SIO_000628
miriam-gene:1950
,
lld:C0026986
;
a
sio:SIO_001121
.
}
dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_provenance
{
dgn-np:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_assertion
dcterms:description
"[Using a probe specific for erb B oncogene, which encodes a truncated form of the EGF receptor, we examined RNA and DNA derived from bone marrow and peripheral blood mononuclear cells from three patients with myelodysplastic syndromes (MDS) and one with acute lymphocytic leukemia (ALL), all bearing an abnormal clone in their bone marrow with a similar unbalanced 1;7 translocation.]. 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:3464613
;
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:NP315420.RAOtDLrf8AaxAcT47cNVvXzl-dh91fiCt1w2vkPukGBys130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:01+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" .
}