@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP968920.RAf02uC6asU4RF0Wx8TVvPbareboFT_dNWvmFam4SxT4M
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP968920.RAf02uC6asU4RF0Wx8TVvPbareboFT_dNWvmFam4SxT4M130_head
{
this:
np:hasAssertion
dgn-np:NP968920.RAf02uC6asU4RF0Wx8TVvPbareboFT_dNWvmFam4SxT4M130_assertion
;
np:hasProvenance
dgn-np:NP968920.RAf02uC6asU4RF0Wx8TVvPbareboFT_dNWvmFam4SxT4M130_provenance
;
np:hasPublicationInfo
dgn-np:NP968920.RAf02uC6asU4RF0Wx8TVvPbareboFT_dNWvmFam4SxT4M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP968920.RAf02uC6asU4RF0Wx8TVvPbareboFT_dNWvmFam4SxT4M130_assertion
a
np:Assertion
.
dgn-np:NP968920.RAf02uC6asU4RF0Wx8TVvPbareboFT_dNWvmFam4SxT4M130_provenance
a
np:Provenance
.
dgn-np:NP968920.RAf02uC6asU4RF0Wx8TVvPbareboFT_dNWvmFam4SxT4M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP968920.RAf02uC6asU4RF0Wx8TVvPbareboFT_dNWvmFam4SxT4M130_assertion
{
miriam-gene:207
a
ncit:C16612
.
lld:C0007138
a
ncit:C7057
.
dgn-gda:DGN6eead4753b2dcb1f4dcaebe219f47ba4
sio:SIO_000628
miriam-gene:207
,
lld:C0007138
;
a
sio:SIO_001121
.
}
dgn-np:NP968920.RAf02uC6asU4RF0Wx8TVvPbareboFT_dNWvmFam4SxT4M130_provenance
{
dgn-np:NP968920.RAf02uC6asU4RF0Wx8TVvPbareboFT_dNWvmFam4SxT4M130_assertion
dcterms:description
"[The relative frequency at which helical domain and kinase domain mutations are found in UC is related to their potency in inducing signaling downstream of AKT and to the phenotypic effects induced in this cell type (E545K>E542K>H1047R).]. 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:22430209
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP968920.RAf02uC6asU4RF0Wx8TVvPbareboFT_dNWvmFam4SxT4M130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:04+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}