@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18
> .
@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:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_head
{
this:
np:hasAssertion
dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_assertion
;
np:hasProvenance
dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_provenance
;
np:hasPublicationInfo
dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_assertion
a
np:Assertion
.
dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_provenance
a
np:Provenance
.
dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C0018923
a
ncit:C7057
.
dgn-gda:DGN4db9579c742c778a4ed24d06d403a435
sio:SIO_000628
miriam-gene:3845
,
lld:C0018923
;
a
sio:SIO_001121
.
}
dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_provenance
{
dgn-np:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_assertion
dcterms:description
"[We studied the occurrence of a specific ras mutation (Asp 13 c-Ki-ras) by oligonucleotide hybridization and the expression of the corresponding p21 protein in tumor tissue and serum by immunohistochemistry and immunoblotting with monoclonal antibodies in five individuals with heavy exposure to VC and resultant angiosarcomas of the liver (ASL).]. 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:8061177
;
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:NP687788.RA5MrB8AJMuV6TlBFWYZSre95jN9t1ZX37dD_orw0go18130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:58+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" .
}