@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE
> .
@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:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_head
{
this:
np:hasAssertion
dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_assertion
;
np:hasProvenance
dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_provenance
;
np:hasPublicationInfo
dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_assertion
a
np:Assertion
.
dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_provenance
a
np:Provenance
.
dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_assertion
{
miriam-gene:3265
a
ncit:C16612
.
lld:C0242379
a
ncit:C7057
.
dgn-gda:DGN2406e4fb98f3984e37045f52d8f9e402
sio:SIO_000628
miriam-gene:3265
,
lld:C0242379
;
a
sio:SIO_001122
.
}
dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_provenance
{
dgn-np:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_assertion
dcterms:description
"[This study suggests that the presence of two rare HRAS1 alleles confers an increased lung cancer risk in Native Hawaiians and Japanese but possibly not in Caucasians. The amino acid replacement of arginine by proline at codon 72 of TP53 appears not to be important in determining lung cancer risk in this population.]. 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:11097227
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP62798.RAtB3U0rDFZOPJl1qQM3Jpehr22q5-uBTuafGjBY2JfJE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:29+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" .
}