@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP805627.RAcshj8jim-pgIGJho33K1OrG5tKn3yF39yvwIMuNIPo4
> .
@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:NP805627.RAcshj8jim-pgIGJho33K1OrG5tKn3yF39yvwIMuNIPo4130_head
{
this:
np:hasAssertion
dgn-np:NP805627.RAcshj8jim-pgIGJho33K1OrG5tKn3yF39yvwIMuNIPo4130_assertion
;
np:hasProvenance
dgn-np:NP805627.RAcshj8jim-pgIGJho33K1OrG5tKn3yF39yvwIMuNIPo4130_provenance
;
np:hasPublicationInfo
dgn-np:NP805627.RAcshj8jim-pgIGJho33K1OrG5tKn3yF39yvwIMuNIPo4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP805627.RAcshj8jim-pgIGJho33K1OrG5tKn3yF39yvwIMuNIPo4130_assertion
a
np:Assertion
.
dgn-np:NP805627.RAcshj8jim-pgIGJho33K1OrG5tKn3yF39yvwIMuNIPo4130_provenance
a
np:Provenance
.
dgn-np:NP805627.RAcshj8jim-pgIGJho33K1OrG5tKn3yF39yvwIMuNIPo4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP805627.RAcshj8jim-pgIGJho33K1OrG5tKn3yF39yvwIMuNIPo4130_assertion
{
miriam-gene:10573
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGNbca923340179190dc2e3a361003e7e8c
sio:SIO_000628
miriam-gene:10573
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP805627.RAcshj8jim-pgIGJho33K1OrG5tKn3yF39yvwIMuNIPo4130_provenance
{
dgn-np:NP805627.RAcshj8jim-pgIGJho33K1OrG5tKn3yF39yvwIMuNIPo4130_assertion
dcterms:description
"[The aims of our study were to analyse alterations in p53, p21, p16 and p15 genes in melanoma tumors and melanoma cell lines by single strand conformational polymorphism (SSCP), and to detect homozygous deletions.]. 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:15960923
;
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:NP805627.RAcshj8jim-pgIGJho33K1OrG5tKn3yF39yvwIMuNIPo4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:14+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" .
}