@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP186488.RAD_8J33994nyI5IDb8v3Q6NwSia0xJONZ7cBQuHCyEk4
> .
@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:NP186488.RAD_8J33994nyI5IDb8v3Q6NwSia0xJONZ7cBQuHCyEk4130_head
{
this:
np:hasAssertion
dgn-np:NP186488.RAD_8J33994nyI5IDb8v3Q6NwSia0xJONZ7cBQuHCyEk4130_assertion
;
np:hasProvenance
dgn-np:NP186488.RAD_8J33994nyI5IDb8v3Q6NwSia0xJONZ7cBQuHCyEk4130_provenance
;
np:hasPublicationInfo
dgn-np:NP186488.RAD_8J33994nyI5IDb8v3Q6NwSia0xJONZ7cBQuHCyEk4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP186488.RAD_8J33994nyI5IDb8v3Q6NwSia0xJONZ7cBQuHCyEk4130_assertion
a
np:Assertion
.
dgn-np:NP186488.RAD_8J33994nyI5IDb8v3Q6NwSia0xJONZ7cBQuHCyEk4130_provenance
a
np:Provenance
.
dgn-np:NP186488.RAD_8J33994nyI5IDb8v3Q6NwSia0xJONZ7cBQuHCyEk4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP186488.RAD_8J33994nyI5IDb8v3Q6NwSia0xJONZ7cBQuHCyEk4130_assertion
{
miriam-gene:657
a
ncit:C16612
.
lld:C0018553
a
ncit:C7057
.
dgn-gda:DGNa4bf3ee8113ca736477ebeb2bf936a07
sio:SIO_000628
miriam-gene:657
,
lld:C0018553
;
a
sio:SIO_001121
.
}
dgn-np:NP186488.RAD_8J33994nyI5IDb8v3Q6NwSia0xJONZ7cBQuHCyEk4130_provenance
{
dgn-np:NP186488.RAD_8J33994nyI5IDb8v3Q6NwSia0xJONZ7cBQuHCyEk4130_assertion
dcterms:description
"[However, the mutation analysis in the PTEN gene and the two other genes involved in juvenile polyposis, namely BMPR1A and MADH4 (SMAD4), in the Cowden syndrome patient failed to show any pathogenic mutation.]. 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:16292097
;
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:NP186488.RAD_8J33994nyI5IDb8v3Q6NwSia0xJONZ7cBQuHCyEk4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:33:42+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: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" .
}