@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis
> .
@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:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_head
{
this:
np:hasAssertion
dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_assertion
;
np:hasProvenance
dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_provenance
;
np:hasPublicationInfo
dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_assertion
a
np:Assertion
.
dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_provenance
a
np:Provenance
.
dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_assertion
{
miriam-gene:3265
a
ncit:C16612
.
lld:C0023418
a
ncit:C7057
.
dgn-gda:DGN63dc54d0e295ccd60d00233d1f093bfe
sio:SIO_000628
miriam-gene:3265
,
lld:C0023418
;
a
sio:SIO_001121
.
}
dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_provenance
{
dgn-np:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_assertion
dcterms:description
"[By using a strategy for analysis of gene mutation based on in vitro amplification of target sequences by the polymerase chain reaction (PCR) and selective oligonucleotide hybridization we analyzed the mutational status of codons 12, 13, and 61 of Ha-ras, K-ras, and N-ras in peripheral blood (PB) and/or bone marrow (BM) in 34 cases of primary MDS.]. 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:3285909
;
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:NP880638.RAWPsT2aPsiXzpFkcLZQvKM2eiWcZGdXH4g3g4PW8cCis130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:58+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" .
}