@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP420961.RAEP_ANvQBEjSVWuy7m89q7Q8f2Re7iMNPPM3pjrWMGdo
> .
@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:NP420961.RAEP_ANvQBEjSVWuy7m89q7Q8f2Re7iMNPPM3pjrWMGdo130_head
{
this:
np:hasAssertion
dgn-np:NP420961.RAEP_ANvQBEjSVWuy7m89q7Q8f2Re7iMNPPM3pjrWMGdo130_assertion
;
np:hasProvenance
dgn-np:NP420961.RAEP_ANvQBEjSVWuy7m89q7Q8f2Re7iMNPPM3pjrWMGdo130_provenance
;
np:hasPublicationInfo
dgn-np:NP420961.RAEP_ANvQBEjSVWuy7m89q7Q8f2Re7iMNPPM3pjrWMGdo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP420961.RAEP_ANvQBEjSVWuy7m89q7Q8f2Re7iMNPPM3pjrWMGdo130_assertion
a
np:Assertion
.
dgn-np:NP420961.RAEP_ANvQBEjSVWuy7m89q7Q8f2Re7iMNPPM3pjrWMGdo130_provenance
a
np:Provenance
.
dgn-np:NP420961.RAEP_ANvQBEjSVWuy7m89q7Q8f2Re7iMNPPM3pjrWMGdo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP420961.RAEP_ANvQBEjSVWuy7m89q7Q8f2Re7iMNPPM3pjrWMGdo130_assertion
{
miriam-gene:5979
a
ncit:C16612
.
lld:C0008073
a
ncit:C7057
.
dgn-gda:DGNf010b26116149afbaa64c566cfec3a16
sio:SIO_000628
miriam-gene:5979
,
lld:C0008073
;
a
sio:SIO_001121
.
}
dgn-np:NP420961.RAEP_ANvQBEjSVWuy7m89q7Q8f2Re7iMNPPM3pjrWMGdo130_provenance
{
dgn-np:NP420961.RAEP_ANvQBEjSVWuy7m89q7Q8f2Re7iMNPPM3pjrWMGdo130_assertion
dcterms:description
"[Two relatively advanced phenomic paradigms are associated with phosphatase and tensin homologue (PTEN) and rearranged during transfection (RET), genes that are associated with cancer predisposition syndromes in addition to developmental disorders.]. 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:17167516
;
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:NP420961.RAEP_ANvQBEjSVWuy7m89q7Q8f2Re7iMNPPM3pjrWMGdo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:10+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" .
}