@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP514562.RAAEr86sQccaX3KF7uQwk9adxAPpC1DV_hSzaQgVwXw0g
> .
@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:NP514562.RAAEr86sQccaX3KF7uQwk9adxAPpC1DV_hSzaQgVwXw0g130_head
{
this:
np:hasAssertion
dgn-np:NP514562.RAAEr86sQccaX3KF7uQwk9adxAPpC1DV_hSzaQgVwXw0g130_assertion
;
np:hasProvenance
dgn-np:NP514562.RAAEr86sQccaX3KF7uQwk9adxAPpC1DV_hSzaQgVwXw0g130_provenance
;
np:hasPublicationInfo
dgn-np:NP514562.RAAEr86sQccaX3KF7uQwk9adxAPpC1DV_hSzaQgVwXw0g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP514562.RAAEr86sQccaX3KF7uQwk9adxAPpC1DV_hSzaQgVwXw0g130_assertion
a
np:Assertion
.
dgn-np:NP514562.RAAEr86sQccaX3KF7uQwk9adxAPpC1DV_hSzaQgVwXw0g130_provenance
a
np:Provenance
.
dgn-np:NP514562.RAAEr86sQccaX3KF7uQwk9adxAPpC1DV_hSzaQgVwXw0g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP514562.RAAEr86sQccaX3KF7uQwk9adxAPpC1DV_hSzaQgVwXw0g130_assertion
{
miriam-gene:4088
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN31f665cadf38db82331212b3f58e4f40
sio:SIO_000628
miriam-gene:4088
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP514562.RAAEr86sQccaX3KF7uQwk9adxAPpC1DV_hSzaQgVwXw0g130_provenance
{
dgn-np:NP514562.RAAEr86sQccaX3KF7uQwk9adxAPpC1DV_hSzaQgVwXw0g130_assertion
dcterms:description
"[The relevance of our results to human cancer is reflected by the fact that human basal cell carcinomas, which almost always harbor activated Hh signaling, have activated TGFβ signaling, as indicated by high levels of phosphorylated SMAD2 and SMAD3 in tumor and stroma.]. 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:20858897
;
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:NP514562.RAAEr86sQccaX3KF7uQwk9adxAPpC1DV_hSzaQgVwXw0g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:06+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" .
}