@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP348284.RAbS6gI0E-JaSdYFRy0dx3aC9GZmwsbcb1N45S2O-lwsw
> .
@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:NP348284.RAbS6gI0E-JaSdYFRy0dx3aC9GZmwsbcb1N45S2O-lwsw130_head
{
this:
np:hasAssertion
dgn-np:NP348284.RAbS6gI0E-JaSdYFRy0dx3aC9GZmwsbcb1N45S2O-lwsw130_assertion
;
np:hasProvenance
dgn-np:NP348284.RAbS6gI0E-JaSdYFRy0dx3aC9GZmwsbcb1N45S2O-lwsw130_provenance
;
np:hasPublicationInfo
dgn-np:NP348284.RAbS6gI0E-JaSdYFRy0dx3aC9GZmwsbcb1N45S2O-lwsw130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP348284.RAbS6gI0E-JaSdYFRy0dx3aC9GZmwsbcb1N45S2O-lwsw130_assertion
a
np:Assertion
.
dgn-np:NP348284.RAbS6gI0E-JaSdYFRy0dx3aC9GZmwsbcb1N45S2O-lwsw130_provenance
a
np:Provenance
.
dgn-np:NP348284.RAbS6gI0E-JaSdYFRy0dx3aC9GZmwsbcb1N45S2O-lwsw130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP348284.RAbS6gI0E-JaSdYFRy0dx3aC9GZmwsbcb1N45S2O-lwsw130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0041107
a
ncit:C7057
.
dgn-gda:DGN537e2abbc687db25ed6f0f3898e12c27
sio:SIO_000628
miriam-gene:7157
,
lld:C0041107
;
a
sio:SIO_001121
.
}
dgn-np:NP348284.RAbS6gI0E-JaSdYFRy0dx3aC9GZmwsbcb1N45S2O-lwsw130_provenance
{
dgn-np:NP348284.RAbS6gI0E-JaSdYFRy0dx3aC9GZmwsbcb1N45S2O-lwsw130_assertion
dcterms:description
"[The evidence for trisomies of 17q with loss of 17p in some cases of neuroblastoma led us to consider whether p53 mutations might contribute to the onset and progression of this malignancy.]. 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:8221661
;
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:NP348284.RAbS6gI0E-JaSdYFRy0dx3aC9GZmwsbcb1N45S2O-lwsw130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:24+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" .
}