@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1001629.RAnztpvuH4257Cn6pNxM_xQDpN96Ip2xqVYNW5bZk7Uxo
> .
@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:NP1001629.RAnztpvuH4257Cn6pNxM_xQDpN96Ip2xqVYNW5bZk7Uxo130_head
{
this:
np:hasAssertion
dgn-np:NP1001629.RAnztpvuH4257Cn6pNxM_xQDpN96Ip2xqVYNW5bZk7Uxo130_assertion
;
np:hasProvenance
dgn-np:NP1001629.RAnztpvuH4257Cn6pNxM_xQDpN96Ip2xqVYNW5bZk7Uxo130_provenance
;
np:hasPublicationInfo
dgn-np:NP1001629.RAnztpvuH4257Cn6pNxM_xQDpN96Ip2xqVYNW5bZk7Uxo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1001629.RAnztpvuH4257Cn6pNxM_xQDpN96Ip2xqVYNW5bZk7Uxo130_assertion
a
np:Assertion
.
dgn-np:NP1001629.RAnztpvuH4257Cn6pNxM_xQDpN96Ip2xqVYNW5bZk7Uxo130_provenance
a
np:Provenance
.
dgn-np:NP1001629.RAnztpvuH4257Cn6pNxM_xQDpN96Ip2xqVYNW5bZk7Uxo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1001629.RAnztpvuH4257Cn6pNxM_xQDpN96Ip2xqVYNW5bZk7Uxo130_assertion
{
miriam-gene:7812
a
ncit:C16612
.
lld:C0023470
a
ncit:C7057
.
dgn-gda:DGN31f55901cf5eeb287987298e4857aa91
sio:SIO_000628
miriam-gene:7812
,
lld:C0023470
;
a
sio:SIO_001121
.
}
dgn-np:NP1001629.RAnztpvuH4257Cn6pNxM_xQDpN96Ip2xqVYNW5bZk7Uxo130_provenance
{
dgn-np:NP1001629.RAnztpvuH4257Cn6pNxM_xQDpN96Ip2xqVYNW5bZk7Uxo130_assertion
dcterms:description
"[Activation of NRas signaling is frequently found in human myeloid leukemia and can be induced by activating mutations as well as by mutations in receptors or signaling molecules upstream of NRas.]. 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:22847614
;
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:NP1001629.RAnztpvuH4257Cn6pNxM_xQDpN96Ip2xqVYNW5bZk7Uxo130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:49:19+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" .
}