@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8
> .
@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:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_head
{
this:
np:hasAssertion
dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_assertion
;
np:hasProvenance
dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_provenance
;
np:hasPublicationInfo
dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_assertion
a
np:Assertion
.
dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_provenance
a
np:Provenance
.
dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_assertion
{
miriam-gene:5624
a
ncit:C16612
.
lld:C0006118
a
ncit:C7057
.
dgn-gda:DGNe1455821fc3a48c9626250f30ca35ba1
sio:SIO_000628
miriam-gene:5624
,
lld:C0006118
;
a
sio:SIO_001121
.
}
dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_provenance
{
dgn-np:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_assertion
dcterms:description
"[The authors analyzed their established hereditary CRC Registry for brain tumors in FAP pedigrees (56 families, 213 individuals), pooled their patients with BTP and known APC mutations with those reported thus far elsewhere, and compared the resulting mutation distribution of FAP-BTP with the mutation distribution for APC mutations in the US.]. 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:17238184
;
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:NP335245.RAuQZNhvk8JUJyyYtCESWHjmROwpK6WlE4pVWJ0cGuoc8130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:17+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" .
}