@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP160347.RAr4V9PQRcv47MrIaD4RHcX9Ucp7E72EnsWofsNCaZ_1I
> .
@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:NP160347.RAr4V9PQRcv47MrIaD4RHcX9Ucp7E72EnsWofsNCaZ_1I130_head
{
this:
np:hasAssertion
dgn-np:NP160347.RAr4V9PQRcv47MrIaD4RHcX9Ucp7E72EnsWofsNCaZ_1I130_assertion
;
np:hasProvenance
dgn-np:NP160347.RAr4V9PQRcv47MrIaD4RHcX9Ucp7E72EnsWofsNCaZ_1I130_provenance
;
np:hasPublicationInfo
dgn-np:NP160347.RAr4V9PQRcv47MrIaD4RHcX9Ucp7E72EnsWofsNCaZ_1I130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP160347.RAr4V9PQRcv47MrIaD4RHcX9Ucp7E72EnsWofsNCaZ_1I130_assertion
a
np:Assertion
.
dgn-np:NP160347.RAr4V9PQRcv47MrIaD4RHcX9Ucp7E72EnsWofsNCaZ_1I130_provenance
a
np:Provenance
.
dgn-np:NP160347.RAr4V9PQRcv47MrIaD4RHcX9Ucp7E72EnsWofsNCaZ_1I130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP160347.RAr4V9PQRcv47MrIaD4RHcX9Ucp7E72EnsWofsNCaZ_1I130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0001430
a
ncit:C7057
.
dgn-gda:DGNd74a70f6c4b2b4fdbc29a0e03fc10f39
sio:SIO_000628
miriam-gene:5624
,
lld:C0001430
;
a
sio:SIO_001121
.
}
dgn-np:NP160347.RAr4V9PQRcv47MrIaD4RHcX9Ucp7E72EnsWofsNCaZ_1I130_provenance
{
dgn-np:NP160347.RAr4V9PQRcv47MrIaD4RHcX9Ucp7E72EnsWofsNCaZ_1I130_assertion
dcterms:description
"[In familial adenomatous polyposis (FAP) syndrome, autosomal dominant inheritance of the mutated APC (adenomatous polyposis coli) gene on chromosome 5q21 typically results in thousands of adenomas in the colorectum and in lesser numbers in the proximal small bowel.]. 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:1335099
;
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:NP160347.RAr4V9PQRcv47MrIaD4RHcX9Ucp7E72EnsWofsNCaZ_1I130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:26+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" .
}