@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo
> .
@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:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_head
{
this:
np:hasAssertion
dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_assertion
;
np:hasProvenance
dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_provenance
;
np:hasPublicationInfo
dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_assertion
a
np:Assertion
.
dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_provenance
a
np:Provenance
.
dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_assertion
{
miriam-gene:5551
a
ncit:C16612
.
lld:C0206180
a
ncit:C7057
.
dgn-gda:DGN7c18de0c76c0e246acb4e9678bfe07d9
sio:SIO_000628
miriam-gene:5551
,
lld:C0206180
;
a
sio:SIO_001121
.
}
dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_provenance
{
dgn-np:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_assertion
dcterms:description
"[Overall, the incidence of PRF1 mutations was found to be significantly higher in patients with ALCL compared with 400 control subjects, among whom only heterozygous A91V was observed in 41 subjects (10.2%) (chi-square test, 10.9; P <.01).]. 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:17477373
;
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:NP477621.RAS8pDWYUVBMVVqnX8EknkZMH7YgRcqfMjVX06R9Zq2Wo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:46+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" .
}