@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1402553.RApWvH_AcNJ1155PCJoNQynaifNnDD76TDnU3MSv8Le3Y
> .
@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:NP1402553.RApWvH_AcNJ1155PCJoNQynaifNnDD76TDnU3MSv8Le3Y130_head
{
this:
np:hasAssertion
dgn-np:NP1402553.RApWvH_AcNJ1155PCJoNQynaifNnDD76TDnU3MSv8Le3Y130_assertion
;
np:hasProvenance
dgn-np:NP1402553.RApWvH_AcNJ1155PCJoNQynaifNnDD76TDnU3MSv8Le3Y130_provenance
;
np:hasPublicationInfo
dgn-np:NP1402553.RApWvH_AcNJ1155PCJoNQynaifNnDD76TDnU3MSv8Le3Y130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1402553.RApWvH_AcNJ1155PCJoNQynaifNnDD76TDnU3MSv8Le3Y130_assertion
a
np:Assertion
.
dgn-np:NP1402553.RApWvH_AcNJ1155PCJoNQynaifNnDD76TDnU3MSv8Le3Y130_provenance
a
np:Provenance
.
dgn-np:NP1402553.RApWvH_AcNJ1155PCJoNQynaifNnDD76TDnU3MSv8Le3Y130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1402553.RApWvH_AcNJ1155PCJoNQynaifNnDD76TDnU3MSv8Le3Y130_assertion
{
miriam-gene:5728
a
ncit:C16612
.
lld:C0018553
a
ncit:C7057
.
dgn-gda:DGN0b41ed40f15c5732e89661bc354ee0d6
sio:SIO_000628
miriam-gene:5728
,
lld:C0018553
;
a
sio:SIO_001121
.
}
dgn-np:NP1402553.RApWvH_AcNJ1155PCJoNQynaifNnDD76TDnU3MSv8Le3Y130_provenance
{
dgn-np:NP1402553.RApWvH_AcNJ1155PCJoNQynaifNnDD76TDnU3MSv8Le3Y130_assertion
dcterms:description
"[The variable and often subtle clinical findings that characterize Cowden Syndrome are frequently unrecognized, raising the possibility that germline PTEN mutations may confer susceptibility to breast cancer in women who have not been diagnosed with this syndrome.]. 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:9715274
;
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:NP1402553.RApWvH_AcNJ1155PCJoNQynaifNnDD76TDnU3MSv8Le3Y130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:22+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" .
}