@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP298594.RAmvJtUI_rVE-OqzoKYvEfKev2WwHRI-Jc3fOoMN0CPI4
> .
@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:NP298594.RAmvJtUI_rVE-OqzoKYvEfKev2WwHRI-Jc3fOoMN0CPI4130_head
{
this:
np:hasAssertion
dgn-np:NP298594.RAmvJtUI_rVE-OqzoKYvEfKev2WwHRI-Jc3fOoMN0CPI4130_assertion
;
np:hasProvenance
dgn-np:NP298594.RAmvJtUI_rVE-OqzoKYvEfKev2WwHRI-Jc3fOoMN0CPI4130_provenance
;
np:hasPublicationInfo
dgn-np:NP298594.RAmvJtUI_rVE-OqzoKYvEfKev2WwHRI-Jc3fOoMN0CPI4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP298594.RAmvJtUI_rVE-OqzoKYvEfKev2WwHRI-Jc3fOoMN0CPI4130_assertion
a
np:Assertion
.
dgn-np:NP298594.RAmvJtUI_rVE-OqzoKYvEfKev2WwHRI-Jc3fOoMN0CPI4130_provenance
a
np:Provenance
.
dgn-np:NP298594.RAmvJtUI_rVE-OqzoKYvEfKev2WwHRI-Jc3fOoMN0CPI4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP298594.RAmvJtUI_rVE-OqzoKYvEfKev2WwHRI-Jc3fOoMN0CPI4130_assertion
{
miriam-gene:1499
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGN3f4a67ddc455e1f3b39d7ebf8d441c04
sio:SIO_000628
miriam-gene:1499
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP298594.RAmvJtUI_rVE-OqzoKYvEfKev2WwHRI-Jc3fOoMN0CPI4130_provenance
{
dgn-np:NP298594.RAmvJtUI_rVE-OqzoKYvEfKev2WwHRI-Jc3fOoMN0CPI4130_assertion
dcterms:description
"[Eight (18%) patients had desmoids that were wild type for CTNNB1 and had no known clinical signs or family history suspicious for FAP at the time of testing or with extended follow up (n = 6).]. 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:22372443
;
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:NP298594.RAmvJtUI_rVE-OqzoKYvEfKev2WwHRI-Jc3fOoMN0CPI4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:49+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" .
}