@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP590315.RAEcN24vOjAClhSdWZ3wbn_kL_BASpa0yDKqbhT8uo0II
> .
@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:NP590315.RAEcN24vOjAClhSdWZ3wbn_kL_BASpa0yDKqbhT8uo0II130_head
{
this:
np:hasAssertion
dgn-np:NP590315.RAEcN24vOjAClhSdWZ3wbn_kL_BASpa0yDKqbhT8uo0II130_assertion
;
np:hasProvenance
dgn-np:NP590315.RAEcN24vOjAClhSdWZ3wbn_kL_BASpa0yDKqbhT8uo0II130_provenance
;
np:hasPublicationInfo
dgn-np:NP590315.RAEcN24vOjAClhSdWZ3wbn_kL_BASpa0yDKqbhT8uo0II130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP590315.RAEcN24vOjAClhSdWZ3wbn_kL_BASpa0yDKqbhT8uo0II130_assertion
a
np:Assertion
.
dgn-np:NP590315.RAEcN24vOjAClhSdWZ3wbn_kL_BASpa0yDKqbhT8uo0II130_provenance
a
np:Provenance
.
dgn-np:NP590315.RAEcN24vOjAClhSdWZ3wbn_kL_BASpa0yDKqbhT8uo0II130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP590315.RAEcN24vOjAClhSdWZ3wbn_kL_BASpa0yDKqbhT8uo0II130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C1959582
a
ncit:C7057
.
dgn-gda:DGN8de6609e40b924720bd94b712f3c1256
sio:SIO_000628
miriam-gene:5728
,
lld:C1959582
;
a
sio:SIO_001121
.
}
dgn-np:NP590315.RAEcN24vOjAClhSdWZ3wbn_kL_BASpa0yDKqbhT8uo0II130_provenance
{
dgn-np:NP590315.RAEcN24vOjAClhSdWZ3wbn_kL_BASpa0yDKqbhT8uo0II130_assertion
dcterms:description
"[Identification of mutations in PTEN in the various disorders that compose the PTEN hamartoma tumor syndrome illustrates just how such genetic knowledge has altered the way we both categorize and manage certain genetic conditions.]. 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:17249301
;
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:NP590315.RAEcN24vOjAClhSdWZ3wbn_kL_BASpa0yDKqbhT8uo0II130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:13+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" .
}