@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP418098.RAWnV_vXEWIEgxdB4zysKI0p-2m4RVSnDUyuke6iHnTDE
> .
@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:NP418098.RAWnV_vXEWIEgxdB4zysKI0p-2m4RVSnDUyuke6iHnTDE130_head
{
this:
np:hasAssertion
dgn-np:NP418098.RAWnV_vXEWIEgxdB4zysKI0p-2m4RVSnDUyuke6iHnTDE130_assertion
;
np:hasProvenance
dgn-np:NP418098.RAWnV_vXEWIEgxdB4zysKI0p-2m4RVSnDUyuke6iHnTDE130_provenance
;
np:hasPublicationInfo
dgn-np:NP418098.RAWnV_vXEWIEgxdB4zysKI0p-2m4RVSnDUyuke6iHnTDE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP418098.RAWnV_vXEWIEgxdB4zysKI0p-2m4RVSnDUyuke6iHnTDE130_assertion
a
np:Assertion
.
dgn-np:NP418098.RAWnV_vXEWIEgxdB4zysKI0p-2m4RVSnDUyuke6iHnTDE130_provenance
a
np:Provenance
.
dgn-np:NP418098.RAWnV_vXEWIEgxdB4zysKI0p-2m4RVSnDUyuke6iHnTDE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP418098.RAWnV_vXEWIEgxdB4zysKI0p-2m4RVSnDUyuke6iHnTDE130_assertion
{
miriam-gene:6794
a
ncit:C16612
.
lld:C0334092
a
ncit:C7057
.
dgn-gda:DGN895cc15e6fc897bbde101bbb84435342
sio:SIO_000628
miriam-gene:6794
,
lld:C0334092
;
a
sio:SIO_001121
.
}
dgn-np:NP418098.RAWnV_vXEWIEgxdB4zysKI0p-2m4RVSnDUyuke6iHnTDE130_provenance
{
dgn-np:NP418098.RAWnV_vXEWIEgxdB4zysKI0p-2m4RVSnDUyuke6iHnTDE130_assertion
dcterms:description
"[Peutz-Jeghers syndrome (PJS) is an autosomal dominant disease caused by germline mutation of the serine threonine kinase 11 and characterized by hamartomatous polyps in the gastrointestinal tract and mucocutaneous melanin pigmentation.]. 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:16616343
;
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:NP418098.RAWnV_vXEWIEgxdB4zysKI0p-2m4RVSnDUyuke6iHnTDE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:08+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" .
}