@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP717579.RAf_ufBtNxXyvdIh2r2Nm6CiOb2yIhl4LU_Aoz6d6KMMI
> .
@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:NP717579.RAf_ufBtNxXyvdIh2r2Nm6CiOb2yIhl4LU_Aoz6d6KMMI130_head
{
this:
np:hasAssertion
dgn-np:NP717579.RAf_ufBtNxXyvdIh2r2Nm6CiOb2yIhl4LU_Aoz6d6KMMI130_assertion
;
np:hasProvenance
dgn-np:NP717579.RAf_ufBtNxXyvdIh2r2Nm6CiOb2yIhl4LU_Aoz6d6KMMI130_provenance
;
np:hasPublicationInfo
dgn-np:NP717579.RAf_ufBtNxXyvdIh2r2Nm6CiOb2yIhl4LU_Aoz6d6KMMI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP717579.RAf_ufBtNxXyvdIh2r2Nm6CiOb2yIhl4LU_Aoz6d6KMMI130_assertion
a
np:Assertion
.
dgn-np:NP717579.RAf_ufBtNxXyvdIh2r2Nm6CiOb2yIhl4LU_Aoz6d6KMMI130_provenance
a
np:Provenance
.
dgn-np:NP717579.RAf_ufBtNxXyvdIh2r2Nm6CiOb2yIhl4LU_Aoz6d6KMMI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP717579.RAf_ufBtNxXyvdIh2r2Nm6CiOb2yIhl4LU_Aoz6d6KMMI130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0023467
a
ncit:C7057
.
dgn-gda:DGN8b311545cfa05c8deab5e8cccba41997
sio:SIO_000628
miriam-gene:7157
,
lld:C0023467
;
a
sio:SIO_001122
.
}
dgn-np:NP717579.RAf_ufBtNxXyvdIh2r2Nm6CiOb2yIhl4LU_Aoz6d6KMMI130_provenance
{
dgn-np:NP717579.RAf_ufBtNxXyvdIh2r2Nm6CiOb2yIhl4LU_Aoz6d6KMMI130_assertion
dcterms:description
"[We previously identified a case of human acute myelogenous leukemia (AML) in which both alleles of the p53 gene had undergone independent missense mutations (at codons 135 cys to ser and 246 met to val).]. 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:1918170
;
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:NP717579.RAf_ufBtNxXyvdIh2r2Nm6CiOb2yIhl4LU_Aoz6d6KMMI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:10+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: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" .
}