@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk
> .
@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:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_head
{
this:
np:hasAssertion
dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_assertion
;
np:hasProvenance
dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_provenance
;
np:hasPublicationInfo
dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_assertion
a
np:Assertion
.
dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_provenance
a
np:Provenance
.
dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_assertion
{
miriam-gene:10544
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGNaf790fb8f7d7a7497f4568770f1db42a
sio:SIO_000628
miriam-gene:10544
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_provenance
{
dgn-np:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_assertion
dcterms:description
"[Using enriched PCR (EPCR), which enables the detection of one mutant allele in the presence of 10,000 normal alleles, we have determined the frequency of mutant ras alleles in the sputum samples of patients with or without lung cancer.]. 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:9027615
;
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:NP490197.RAw6cFlir9Xy4eqBrDXtDGUNeyzn8TAASJWYcsoeOgYJk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:53+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" .
}