@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP579988.RAkQe7vwqyzyQQRfNJXUUDk7FfixHSV2mUTVT1QaUs7Rs
> .
@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/v3.0.0/void/
> .
dgn-np:NP579988.RAkQe7vwqyzyQQRfNJXUUDk7FfixHSV2mUTVT1QaUs7Rs130_head
{
this:
np:hasAssertion
dgn-np:NP579988.RAkQe7vwqyzyQQRfNJXUUDk7FfixHSV2mUTVT1QaUs7Rs130_assertion
;
np:hasProvenance
dgn-np:NP579988.RAkQe7vwqyzyQQRfNJXUUDk7FfixHSV2mUTVT1QaUs7Rs130_provenance
;
np:hasPublicationInfo
dgn-np:NP579988.RAkQe7vwqyzyQQRfNJXUUDk7FfixHSV2mUTVT1QaUs7Rs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP579988.RAkQe7vwqyzyQQRfNJXUUDk7FfixHSV2mUTVT1QaUs7Rs130_assertion
a
np:Assertion
.
dgn-np:NP579988.RAkQe7vwqyzyQQRfNJXUUDk7FfixHSV2mUTVT1QaUs7Rs130_provenance
a
np:Provenance
.
dgn-np:NP579988.RAkQe7vwqyzyQQRfNJXUUDk7FfixHSV2mUTVT1QaUs7Rs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP579988.RAkQe7vwqyzyQQRfNJXUUDk7FfixHSV2mUTVT1QaUs7Rs130_assertion
{
miriam-gene:4595
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGNb4a4821bee5ada4f468debf6de552146
sio:SIO_000628
miriam-gene:4595
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP579988.RAkQe7vwqyzyQQRfNJXUUDk7FfixHSV2mUTVT1QaUs7Rs130_provenance
{
dgn-np:NP579988.RAkQe7vwqyzyQQRfNJXUUDk7FfixHSV2mUTVT1QaUs7Rs130_assertion
dcterms:description
"[This report expands the phenotype known to be related to AXIN2 alterations and raises the question of whether to screen AXIN2 in FAP cases negative for alterations in APC and MUTYH.]. 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:23838596
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP579988.RAkQe7vwqyzyQQRfNJXUUDk7FfixHSV2mUTVT1QaUs7Rs130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:43:25+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}