@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP257135.RAIdA7I64KItooayiQ6wSWEiTWJsXhpUJ0XEsVNlKjHyI
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP257135.RAIdA7I64KItooayiQ6wSWEiTWJsXhpUJ0XEsVNlKjHyI130_head
{
this:
np:hasAssertion
dgn-np:NP257135.RAIdA7I64KItooayiQ6wSWEiTWJsXhpUJ0XEsVNlKjHyI130_assertion
;
np:hasProvenance
dgn-np:NP257135.RAIdA7I64KItooayiQ6wSWEiTWJsXhpUJ0XEsVNlKjHyI130_provenance
;
np:hasPublicationInfo
dgn-np:NP257135.RAIdA7I64KItooayiQ6wSWEiTWJsXhpUJ0XEsVNlKjHyI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP257135.RAIdA7I64KItooayiQ6wSWEiTWJsXhpUJ0XEsVNlKjHyI130_assertion
a
np:Assertion
.
dgn-np:NP257135.RAIdA7I64KItooayiQ6wSWEiTWJsXhpUJ0XEsVNlKjHyI130_provenance
a
np:Provenance
.
dgn-np:NP257135.RAIdA7I64KItooayiQ6wSWEiTWJsXhpUJ0XEsVNlKjHyI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP257135.RAIdA7I64KItooayiQ6wSWEiTWJsXhpUJ0XEsVNlKjHyI130_assertion
{
miriam-gene:1499
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGN4c338fe444506372bb32b9141f79bc04
sio:SIO_000628
miriam-gene:1499
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP257135.RAIdA7I64KItooayiQ6wSWEiTWJsXhpUJ0XEsVNlKjHyI130_provenance
{
dgn-np:NP257135.RAIdA7I64KItooayiQ6wSWEiTWJsXhpUJ0XEsVNlKjHyI130_assertion
dcterms:description
"[Our results indicate that APC germline mutations are frequent but CTNNB1 germline mutations are rare in FAP patients, suggesting that CTNNB1 mutation cannot substitute for APC mutation in the initiation of FAP.]. 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:10398435
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP257135.RAIdA7I64KItooayiQ6wSWEiTWJsXhpUJ0XEsVNlKjHyI130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:42+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}