@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP924215.RARHOGeiHfW34L8L0egkjU7tvK5ivpTb7gH8eyCWznxwI
> .
@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:NP924215.RARHOGeiHfW34L8L0egkjU7tvK5ivpTb7gH8eyCWznxwI130_head
{
this:
np:hasAssertion
dgn-np:NP924215.RARHOGeiHfW34L8L0egkjU7tvK5ivpTb7gH8eyCWznxwI130_assertion
;
np:hasProvenance
dgn-np:NP924215.RARHOGeiHfW34L8L0egkjU7tvK5ivpTb7gH8eyCWznxwI130_provenance
;
np:hasPublicationInfo
dgn-np:NP924215.RARHOGeiHfW34L8L0egkjU7tvK5ivpTb7gH8eyCWznxwI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP924215.RARHOGeiHfW34L8L0egkjU7tvK5ivpTb7gH8eyCWznxwI130_assertion
a
np:Assertion
.
dgn-np:NP924215.RARHOGeiHfW34L8L0egkjU7tvK5ivpTb7gH8eyCWznxwI130_provenance
a
np:Provenance
.
dgn-np:NP924215.RARHOGeiHfW34L8L0egkjU7tvK5ivpTb7gH8eyCWznxwI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP924215.RARHOGeiHfW34L8L0egkjU7tvK5ivpTb7gH8eyCWznxwI130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0017097
a
ncit:C7057
.
dgn-gda:DGN880aa4ea16b52c5c2f9ce1a962739513
sio:SIO_000628
miriam-gene:5624
,
lld:C0017097
;
a
sio:SIO_001121
.
}
dgn-np:NP924215.RARHOGeiHfW34L8L0egkjU7tvK5ivpTb7gH8eyCWznxwI130_provenance
{
dgn-np:NP924215.RARHOGeiHfW34L8L0egkjU7tvK5ivpTb7gH8eyCWznxwI130_assertion
dcterms:description
"[This disorder was regarded as a separate disease until the identification of the APC gene when it was recognized that mutations in the APC gene were the underlying cause of both Gardner syndrome and familial adenomatous polyposis (FAP).]. 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:16411234
;
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:NP924215.RARHOGeiHfW34L8L0egkjU7tvK5ivpTb7gH8eyCWznxwI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:27+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" .
}