@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP908489.RAgINJ4vIJhPc0pZ7R-znifCG9bd-Sh8CJE-vfhX4jv1M
> .
@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:NP908489.RAgINJ4vIJhPc0pZ7R-znifCG9bd-Sh8CJE-vfhX4jv1M130_head
{
this:
np:hasAssertion
dgn-np:NP908489.RAgINJ4vIJhPc0pZ7R-znifCG9bd-Sh8CJE-vfhX4jv1M130_assertion
;
np:hasProvenance
dgn-np:NP908489.RAgINJ4vIJhPc0pZ7R-znifCG9bd-Sh8CJE-vfhX4jv1M130_provenance
;
np:hasPublicationInfo
dgn-np:NP908489.RAgINJ4vIJhPc0pZ7R-znifCG9bd-Sh8CJE-vfhX4jv1M130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP908489.RAgINJ4vIJhPc0pZ7R-znifCG9bd-Sh8CJE-vfhX4jv1M130_assertion
a
np:Assertion
.
dgn-np:NP908489.RAgINJ4vIJhPc0pZ7R-znifCG9bd-Sh8CJE-vfhX4jv1M130_provenance
a
np:Provenance
.
dgn-np:NP908489.RAgINJ4vIJhPc0pZ7R-znifCG9bd-Sh8CJE-vfhX4jv1M130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP908489.RAgINJ4vIJhPc0pZ7R-znifCG9bd-Sh8CJE-vfhX4jv1M130_assertion
{
miriam-gene:3845
a
ncit:C16612
.
lld:C0677898
a
ncit:C7057
.
dgn-gda:DGNb338ce47ff72865d7671c509b9c52d44
sio:SIO_000628
miriam-gene:3845
,
lld:C0677898
;
a
sio:SIO_001121
.
}
dgn-np:NP908489.RAgINJ4vIJhPc0pZ7R-znifCG9bd-Sh8CJE-vfhX4jv1M130_provenance
{
dgn-np:NP908489.RAgINJ4vIJhPc0pZ7R-znifCG9bd-Sh8CJE-vfhX4jv1M130_assertion
dcterms:description
"[Transition from the precursor lesion to an invasive cancer is associated with gain of the short arm of chromosome 12, in which multiple genes might be involved, including KRAS2 and possibly NANOG (pseudogenes).]. 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:21564133
;
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:NP908489.RAgINJ4vIJhPc0pZ7R-znifCG9bd-Sh8CJE-vfhX4jv1M130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:17+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" .
}