@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP48555.RAdB2ctiIb2CaNrQtNQLrEzfaTj15ohyxqwGium8ZUPFQ
> .
@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:NP48555.RAdB2ctiIb2CaNrQtNQLrEzfaTj15ohyxqwGium8ZUPFQ130_head
{
this:
np:hasAssertion
dgn-np:NP48555.RAdB2ctiIb2CaNrQtNQLrEzfaTj15ohyxqwGium8ZUPFQ130_assertion
;
np:hasProvenance
dgn-np:NP48555.RAdB2ctiIb2CaNrQtNQLrEzfaTj15ohyxqwGium8ZUPFQ130_provenance
;
np:hasPublicationInfo
dgn-np:NP48555.RAdB2ctiIb2CaNrQtNQLrEzfaTj15ohyxqwGium8ZUPFQ130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP48555.RAdB2ctiIb2CaNrQtNQLrEzfaTj15ohyxqwGium8ZUPFQ130_assertion
a
np:Assertion
.
dgn-np:NP48555.RAdB2ctiIb2CaNrQtNQLrEzfaTj15ohyxqwGium8ZUPFQ130_provenance
a
np:Provenance
.
dgn-np:NP48555.RAdB2ctiIb2CaNrQtNQLrEzfaTj15ohyxqwGium8ZUPFQ130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP48555.RAdB2ctiIb2CaNrQtNQLrEzfaTj15ohyxqwGium8ZUPFQ130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGN68f70bfbef06b5229fe9cac977b53cb8
sio:SIO_000628
miriam-gene:324
,
lld:C0032580
;
a
sio:SIO_001122
.
}
dgn-np:NP48555.RAdB2ctiIb2CaNrQtNQLrEzfaTj15ohyxqwGium8ZUPFQ130_provenance
{
dgn-np:NP48555.RAdB2ctiIb2CaNrQtNQLrEzfaTj15ohyxqwGium8ZUPFQ130_assertion
dcterms:description
"[While germline mutations in the adenomatous polyposis coli (APC) gene cause the hereditary colon cancer syndrome (familial adenomatous polyposis (FAP)), the role of common germline APC variants in sporadic adenomatous polyposis remains unclear.]. 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:20510605
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP48555.RAdB2ctiIb2CaNrQtNQLrEzfaTj15ohyxqwGium8ZUPFQ130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:22+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" .
}