@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP406288.RAohj6ydj2p9opjcuWAdF4evgWwegHTAakOkMA5B8Hrxo
> .
@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:NP406288.RAohj6ydj2p9opjcuWAdF4evgWwegHTAakOkMA5B8Hrxo130_head
{
this:
np:hasAssertion
dgn-np:NP406288.RAohj6ydj2p9opjcuWAdF4evgWwegHTAakOkMA5B8Hrxo130_assertion
;
np:hasProvenance
dgn-np:NP406288.RAohj6ydj2p9opjcuWAdF4evgWwegHTAakOkMA5B8Hrxo130_provenance
;
np:hasPublicationInfo
dgn-np:NP406288.RAohj6ydj2p9opjcuWAdF4evgWwegHTAakOkMA5B8Hrxo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP406288.RAohj6ydj2p9opjcuWAdF4evgWwegHTAakOkMA5B8Hrxo130_assertion
a
np:Assertion
.
dgn-np:NP406288.RAohj6ydj2p9opjcuWAdF4evgWwegHTAakOkMA5B8Hrxo130_provenance
a
np:Provenance
.
dgn-np:NP406288.RAohj6ydj2p9opjcuWAdF4evgWwegHTAakOkMA5B8Hrxo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP406288.RAohj6ydj2p9opjcuWAdF4evgWwegHTAakOkMA5B8Hrxo130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0019247
a
ncit:C7057
.
dgn-gda:DGN11fd7968099e8a1b193e55c285381648
sio:SIO_000628
miriam-gene:324
,
lld:C0019247
;
a
sio:SIO_001121
.
}
dgn-np:NP406288.RAohj6ydj2p9opjcuWAdF4evgWwegHTAakOkMA5B8Hrxo130_provenance
{
dgn-np:NP406288.RAohj6ydj2p9opjcuWAdF4evgWwegHTAakOkMA5B8Hrxo130_assertion
dcterms:description
"[Loss of function of both alleles of the APC gene results in colorectal adenoma formation in familial adenomatous polyposis, an autosomal dominant genetic disorder leading to multiple colorectal tumors at an early age.]. 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:9012454
;
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:NP406288.RAohj6ydj2p9opjcuWAdF4evgWwegHTAakOkMA5B8Hrxo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:01+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" .
}