@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_head
{
this:
np:hasAssertion
dgn-np:NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_assertion
;
np:hasProvenance
dgn-np:NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_provenance
;
np:hasPublicationInfo
dgn-np:NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_assertion
a
np:Assertion
.
dgn-np:NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_provenance
a
np:Provenance
.
dgn-np:NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_assertion
{
miriam-gene:2187
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN5d2918b7eba24170896d3417b4c5e73b
sio:SIO_000628
miriam-gene:2187
,
lld:C0023467
;
a
sio:SIO_001121
.
}
dgn-np:NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_provenance
{
dgn-np:NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_assertion
dcterms:description
"[In the present report, we extend our analysis of p53 gene mutations to 70 cases of AML representative of the other FAB types of the disease, including M1 (16 cases), M2 (20 cases), M4 (17 cases), M5 (12 cases), and M6 (5 cases).]. 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:8037181
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1330477.RArwXlAD238nN9CyNwQwcOmnzSfJP5K5O1GiOlsd4OBK0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:51:49+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}