@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP184302.RAgpVaCBlCvrAXGI5yEBk38rSZywadvmlf3Z-yOknJ-z4
> .
@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:NP184302.RAgpVaCBlCvrAXGI5yEBk38rSZywadvmlf3Z-yOknJ-z4130_head
{
this:
np:hasAssertion
dgn-np:NP184302.RAgpVaCBlCvrAXGI5yEBk38rSZywadvmlf3Z-yOknJ-z4130_assertion
;
np:hasProvenance
dgn-np:NP184302.RAgpVaCBlCvrAXGI5yEBk38rSZywadvmlf3Z-yOknJ-z4130_provenance
;
np:hasPublicationInfo
dgn-np:NP184302.RAgpVaCBlCvrAXGI5yEBk38rSZywadvmlf3Z-yOknJ-z4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP184302.RAgpVaCBlCvrAXGI5yEBk38rSZywadvmlf3Z-yOknJ-z4130_assertion
a
np:Assertion
.
dgn-np:NP184302.RAgpVaCBlCvrAXGI5yEBk38rSZywadvmlf3Z-yOknJ-z4130_provenance
a
np:Provenance
.
dgn-np:NP184302.RAgpVaCBlCvrAXGI5yEBk38rSZywadvmlf3Z-yOknJ-z4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP184302.RAgpVaCBlCvrAXGI5yEBk38rSZywadvmlf3Z-yOknJ-z4130_assertion
{
miriam-gene:7157
a
ncit:C16612
.
lld:C0684249
a
ncit:C7057
.
dgn-gda:DGN5d3d2a23c2fb42322d8a330be9079c3c
sio:SIO_000628
miriam-gene:7157
,
lld:C0684249
;
a
sio:SIO_001121
.
}
dgn-np:NP184302.RAgpVaCBlCvrAXGI5yEBk38rSZywadvmlf3Z-yOknJ-z4130_provenance
{
dgn-np:NP184302.RAgpVaCBlCvrAXGI5yEBk38rSZywadvmlf3Z-yOknJ-z4130_assertion
dcterms:description
"[Although the short arm of chromosome 17, which contains the p53 gene, is frequently affected by loss of heterozygosity (LOH) in lung cancer, little is known about similar changes on the long arm.]. 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:7671234
;
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:NP184302.RAgpVaCBlCvrAXGI5yEBk38rSZywadvmlf3Z-yOknJ-z4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:39+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" .
}