@prefix dct: <
http://purl.org/dc/terms/
> .
@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP936115.RAMvPVLGUL8ZfI2hU76dVxD9HzAfa3kuaXk96Qe90yluY
> .
@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 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:NP936115.RAMvPVLGUL8ZfI2hU76dVxD9HzAfa3kuaXk96Qe90yluY130_head
{
this:
np:hasAssertion
dgn-np:NP936115.RAMvPVLGUL8ZfI2hU76dVxD9HzAfa3kuaXk96Qe90yluY130_assertion
;
np:hasProvenance
dgn-np:NP936115.RAMvPVLGUL8ZfI2hU76dVxD9HzAfa3kuaXk96Qe90yluY130_provenance
;
np:hasPublicationInfo
dgn-np:NP936115.RAMvPVLGUL8ZfI2hU76dVxD9HzAfa3kuaXk96Qe90yluY130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP936115.RAMvPVLGUL8ZfI2hU76dVxD9HzAfa3kuaXk96Qe90yluY130_assertion
a
np:Assertion
.
dgn-np:NP936115.RAMvPVLGUL8ZfI2hU76dVxD9HzAfa3kuaXk96Qe90yluY130_provenance
a
np:Provenance
.
dgn-np:NP936115.RAMvPVLGUL8ZfI2hU76dVxD9HzAfa3kuaXk96Qe90yluY130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP936115.RAMvPVLGUL8ZfI2hU76dVxD9HzAfa3kuaXk96Qe90yluY130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0086692
a
ncit:C7057
.
dgn-gda:DGNefdb614cf038a81167f4d3eec8676766
sio:SIO_000628
miriam-gene:324
,
lld:C0086692
;
a
sio:SIO_001121
.
}
dgn-np:NP936115.RAMvPVLGUL8ZfI2hU76dVxD9HzAfa3kuaXk96Qe90yluY130_provenance
{
dgn-np:NP936115.RAMvPVLGUL8ZfI2hU76dVxD9HzAfa3kuaXk96Qe90yluY130_assertion
dct:description
"[The present results and our previous data on LOH in a recurring desmoid tumor suggest that the heterozygous mutant/wild-type condition of the APC gene may give rise to benign tumors, and that functional loss of this gene leads to development of tumors not only in the colon but also in other various parts of the body in FAP patients.]. 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:1351034
;
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:NP936115.RAMvPVLGUL8ZfI2hU76dVxD9HzAfa3kuaXk96Qe90yluY130_publicationInfo
{
this:
dct:created
"2014-10-02T12:41:33+02:00"^^
xsd:dateTime
;
dct:rights
<
http://opendatacommons.org/licenses/odbl/1.0/
> ;
dct:rightsHolder
dgn-void:IBIGroup
;
dct: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" .
}