@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP471593.RAexXk-bbRcxf4VG1Bb9Y_dwK1u1oQq0Eqp_tQOLgftMg
> .
@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:NP471593.RAexXk-bbRcxf4VG1Bb9Y_dwK1u1oQq0Eqp_tQOLgftMg130_head
{
this:
np:hasAssertion
dgn-np:NP471593.RAexXk-bbRcxf4VG1Bb9Y_dwK1u1oQq0Eqp_tQOLgftMg130_assertion
;
np:hasProvenance
dgn-np:NP471593.RAexXk-bbRcxf4VG1Bb9Y_dwK1u1oQq0Eqp_tQOLgftMg130_provenance
;
np:hasPublicationInfo
dgn-np:NP471593.RAexXk-bbRcxf4VG1Bb9Y_dwK1u1oQq0Eqp_tQOLgftMg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP471593.RAexXk-bbRcxf4VG1Bb9Y_dwK1u1oQq0Eqp_tQOLgftMg130_assertion
a
np:Assertion
.
dgn-np:NP471593.RAexXk-bbRcxf4VG1Bb9Y_dwK1u1oQq0Eqp_tQOLgftMg130_provenance
a
np:Provenance
.
dgn-np:NP471593.RAexXk-bbRcxf4VG1Bb9Y_dwK1u1oQq0Eqp_tQOLgftMg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP471593.RAexXk-bbRcxf4VG1Bb9Y_dwK1u1oQq0Eqp_tQOLgftMg130_assertion
{
miriam-gene:6690
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN6ec04c64ad7dc19d6824172a6a4ea824
sio:SIO_000628
miriam-gene:6690
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP471593.RAexXk-bbRcxf4VG1Bb9Y_dwK1u1oQq0Eqp_tQOLgftMg130_provenance
{
dgn-np:NP471593.RAexXk-bbRcxf4VG1Bb9Y_dwK1u1oQq0Eqp_tQOLgftMg130_assertion
dcterms:description
"[Although this case does not meet the classic criteria of hereditary pancreatitis, it does suggest that the SPINK1 N34S mutation may be associated with cancer development in patients with hereditary pancreatitis.]. 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:15084977
;
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:NP471593.RAexXk-bbRcxf4VG1Bb9Y_dwK1u1oQq0Eqp_tQOLgftMg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:42+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" .
}