@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP565542.RAoEOvDnnkZBFWssqEvKE5h-YmiNe6Z7QlLvCDUq7so1s
> .
@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:NP565542.RAoEOvDnnkZBFWssqEvKE5h-YmiNe6Z7QlLvCDUq7so1s130_head
{
this:
np:hasAssertion
dgn-np:NP565542.RAoEOvDnnkZBFWssqEvKE5h-YmiNe6Z7QlLvCDUq7so1s130_assertion
;
np:hasProvenance
dgn-np:NP565542.RAoEOvDnnkZBFWssqEvKE5h-YmiNe6Z7QlLvCDUq7so1s130_provenance
;
np:hasPublicationInfo
dgn-np:NP565542.RAoEOvDnnkZBFWssqEvKE5h-YmiNe6Z7QlLvCDUq7so1s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP565542.RAoEOvDnnkZBFWssqEvKE5h-YmiNe6Z7QlLvCDUq7so1s130_assertion
a
np:Assertion
.
dgn-np:NP565542.RAoEOvDnnkZBFWssqEvKE5h-YmiNe6Z7QlLvCDUq7so1s130_provenance
a
np:Provenance
.
dgn-np:NP565542.RAoEOvDnnkZBFWssqEvKE5h-YmiNe6Z7QlLvCDUq7so1s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP565542.RAoEOvDnnkZBFWssqEvKE5h-YmiNe6Z7QlLvCDUq7so1s130_assertion
{
miriam-gene:7453
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGN05763c864d7b201931baff0639811e80
sio:SIO_000628
miriam-gene:7453
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP565542.RAoEOvDnnkZBFWssqEvKE5h-YmiNe6Z7QlLvCDUq7so1s130_provenance
{
dgn-np:NP565542.RAoEOvDnnkZBFWssqEvKE5h-YmiNe6Z7QlLvCDUq7so1s130_assertion
dcterms:description
"[These data suggest that concurrent p16 upregulation and decreased proliferation are more general phenomena in different types of invasive growth patterns in basal cell carcinomas and that these only partially overlap with the gamma 2 chain of laminin-332 associated invasion patterns.]. 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:17370299
;
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:NP565542.RAoEOvDnnkZBFWssqEvKE5h-YmiNe6Z7QlLvCDUq7so1s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:41+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" .
}