@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP415537.RAMfIQuSCc37JWGeuUdSk3Q4opdV0iaZl39a89qE2s7eE
> .
@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:NP415537.RAMfIQuSCc37JWGeuUdSk3Q4opdV0iaZl39a89qE2s7eE130_head
{
this:
np:hasAssertion
dgn-np:NP415537.RAMfIQuSCc37JWGeuUdSk3Q4opdV0iaZl39a89qE2s7eE130_assertion
;
np:hasProvenance
dgn-np:NP415537.RAMfIQuSCc37JWGeuUdSk3Q4opdV0iaZl39a89qE2s7eE130_provenance
;
np:hasPublicationInfo
dgn-np:NP415537.RAMfIQuSCc37JWGeuUdSk3Q4opdV0iaZl39a89qE2s7eE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP415537.RAMfIQuSCc37JWGeuUdSk3Q4opdV0iaZl39a89qE2s7eE130_assertion
a
np:Assertion
.
dgn-np:NP415537.RAMfIQuSCc37JWGeuUdSk3Q4opdV0iaZl39a89qE2s7eE130_provenance
a
np:Provenance
.
dgn-np:NP415537.RAMfIQuSCc37JWGeuUdSk3Q4opdV0iaZl39a89qE2s7eE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP415537.RAMfIQuSCc37JWGeuUdSk3Q4opdV0iaZl39a89qE2s7eE130_assertion
{
miriam-gene:10923
a
ncit:C16612
.
lld:C0035335
a
ncit:C7057
.
dgn-gda:DGN47534790ad4f23a39f1890bbd1a76219
sio:SIO_000628
miriam-gene:10923
,
lld:C0035335
;
a
sio:SIO_001121
.
}
dgn-np:NP415537.RAMfIQuSCc37JWGeuUdSk3Q4opdV0iaZl39a89qE2s7eE130_provenance
{
dgn-np:NP415537.RAMfIQuSCc37JWGeuUdSk3Q4opdV0iaZl39a89qE2s7eE130_assertion
dcterms:description
"[These findings suggest that alterations in the p53, p16, and p15 genes are common in human pancreatic cancer cell lines, while p53 or RB mutations are common in hepatoma cell lines.]. 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:9058294
;
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:NP415537.RAMfIQuSCc37JWGeuUdSk3Q4opdV0iaZl39a89qE2s7eE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:07+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" .
}