@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP470581.RA0kYEw9v2NC2h5bvZIS0re4dEDp3lO1lr3vzPcWgl-z8
> .
@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:NP470581.RA0kYEw9v2NC2h5bvZIS0re4dEDp3lO1lr3vzPcWgl-z8130_head
{
this:
np:hasAssertion
dgn-np:NP470581.RA0kYEw9v2NC2h5bvZIS0re4dEDp3lO1lr3vzPcWgl-z8130_assertion
;
np:hasProvenance
dgn-np:NP470581.RA0kYEw9v2NC2h5bvZIS0re4dEDp3lO1lr3vzPcWgl-z8130_provenance
;
np:hasPublicationInfo
dgn-np:NP470581.RA0kYEw9v2NC2h5bvZIS0re4dEDp3lO1lr3vzPcWgl-z8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP470581.RA0kYEw9v2NC2h5bvZIS0re4dEDp3lO1lr3vzPcWgl-z8130_assertion
a
np:Assertion
.
dgn-np:NP470581.RA0kYEw9v2NC2h5bvZIS0re4dEDp3lO1lr3vzPcWgl-z8130_provenance
a
np:Provenance
.
dgn-np:NP470581.RA0kYEw9v2NC2h5bvZIS0re4dEDp3lO1lr3vzPcWgl-z8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP470581.RA0kYEw9v2NC2h5bvZIS0re4dEDp3lO1lr3vzPcWgl-z8130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0024314
a
ncit:C7057
.
dgn-gda:DGNfe8084f5bb3dcf7f8e5f8137e01b9932
sio:SIO_000628
miriam-gene:7157
,
lld:C0024314
;
a
sio:SIO_001121
.
}
dgn-np:NP470581.RA0kYEw9v2NC2h5bvZIS0re4dEDp3lO1lr3vzPcWgl-z8130_provenance
{
dgn-np:NP470581.RA0kYEw9v2NC2h5bvZIS0re4dEDp3lO1lr3vzPcWgl-z8130_assertion
dcterms:description
"[From these findings and from data available in the literature the conclusion can be drawn that p53 gene mutations at codons 158 and 167 may be associated with lymphoproliferative disorders and that low- or intermediate-grade NHL, including leukemic mantle cell lymphoma, may frequently carry this genetic change.]. 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:8603336
;
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:NP470581.RA0kYEw9v2NC2h5bvZIS0re4dEDp3lO1lr3vzPcWgl-z8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:42+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" .
}