@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP386056.RAP4F8V-U9HJVbUXH6lQF-J4nCJFvCLRR0Eoy1mcYFOxk
> .
@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:NP386056.RAP4F8V-U9HJVbUXH6lQF-J4nCJFvCLRR0Eoy1mcYFOxk130_head
{
this:
np:hasAssertion
dgn-np:NP386056.RAP4F8V-U9HJVbUXH6lQF-J4nCJFvCLRR0Eoy1mcYFOxk130_assertion
;
np:hasProvenance
dgn-np:NP386056.RAP4F8V-U9HJVbUXH6lQF-J4nCJFvCLRR0Eoy1mcYFOxk130_provenance
;
np:hasPublicationInfo
dgn-np:NP386056.RAP4F8V-U9HJVbUXH6lQF-J4nCJFvCLRR0Eoy1mcYFOxk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP386056.RAP4F8V-U9HJVbUXH6lQF-J4nCJFvCLRR0Eoy1mcYFOxk130_assertion
a
np:Assertion
.
dgn-np:NP386056.RAP4F8V-U9HJVbUXH6lQF-J4nCJFvCLRR0Eoy1mcYFOxk130_provenance
a
np:Provenance
.
dgn-np:NP386056.RAP4F8V-U9HJVbUXH6lQF-J4nCJFvCLRR0Eoy1mcYFOxk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP386056.RAP4F8V-U9HJVbUXH6lQF-J4nCJFvCLRR0Eoy1mcYFOxk130_assertion
{
miriam-gene:1630
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN6f09d2a010518c07da32c57b0a85061b
sio:SIO_000628
miriam-gene:1630
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP386056.RAP4F8V-U9HJVbUXH6lQF-J4nCJFvCLRR0Eoy1mcYFOxk130_provenance
{
dgn-np:NP386056.RAP4F8V-U9HJVbUXH6lQF-J4nCJFvCLRR0Eoy1mcYFOxk130_assertion
dcterms:description
"[A series of molecular changes including loss of heterozygosity (LOH) at 17p (TP53 gene), 13q (RB gene), 18q (DCC gene), and 9p21 (CDKN2a gene) chromosomal regions have been identified in dysplasias, carcinomas in situ, and invasive carcinomas of the gallbladder, whereas mutations in K- and N-ras genes are rare.]. 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:9923922
;
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:NP386056.RAP4F8V-U9HJVbUXH6lQF-J4nCJFvCLRR0Eoy1mcYFOxk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:50+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" .
}