@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP549704.RAPY04QQVKDxUG4JwOQCK25zxD2siELHXHbASwVItImH8
> .
@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:NP549704.RAPY04QQVKDxUG4JwOQCK25zxD2siELHXHbASwVItImH8130_head
{
this:
np:hasAssertion
dgn-np:NP549704.RAPY04QQVKDxUG4JwOQCK25zxD2siELHXHbASwVItImH8130_assertion
;
np:hasProvenance
dgn-np:NP549704.RAPY04QQVKDxUG4JwOQCK25zxD2siELHXHbASwVItImH8130_provenance
;
np:hasPublicationInfo
dgn-np:NP549704.RAPY04QQVKDxUG4JwOQCK25zxD2siELHXHbASwVItImH8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP549704.RAPY04QQVKDxUG4JwOQCK25zxD2siELHXHbASwVItImH8130_assertion
a
np:Assertion
.
dgn-np:NP549704.RAPY04QQVKDxUG4JwOQCK25zxD2siELHXHbASwVItImH8130_provenance
a
np:Provenance
.
dgn-np:NP549704.RAPY04QQVKDxUG4JwOQCK25zxD2siELHXHbASwVItImH8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP549704.RAPY04QQVKDxUG4JwOQCK25zxD2siELHXHbASwVItImH8130_assertion
{
miriam-gene:4583
a
ncit:C16612
.
lld:C1518869
a
ncit:C7057
.
dgn-gda:DGN4181974a3f4228e23d10d284729f2181
sio:SIO_000628
miriam-gene:4583
,
lld:C1518869
;
a
sio:SIO_001121
.
}
dgn-np:NP549704.RAPY04QQVKDxUG4JwOQCK25zxD2siELHXHbASwVItImH8130_provenance
{
dgn-np:NP549704.RAPY04QQVKDxUG4JwOQCK25zxD2siELHXHbASwVItImH8130_assertion
dcterms:description
"[K-ras mutation and the expression of S100A4 and MUC2 (especially in intestinal subtype) were found to be related to malignancy in IPMN, and may be useful for the diagnosis and for assessing the biological behavior of IPMN.]. 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:19412570
;
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:NP549704.RAPY04QQVKDxUG4JwOQCK25zxD2siELHXHbASwVItImH8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:31+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" .
}