@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP438839.RA645r-53oUn3Ttu0uJ8U506D8vFcxpohoZxtTB6L-9OI
> .
@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:NP438839.RA645r-53oUn3Ttu0uJ8U506D8vFcxpohoZxtTB6L-9OI130_head
{
this:
np:hasAssertion
dgn-np:NP438839.RA645r-53oUn3Ttu0uJ8U506D8vFcxpohoZxtTB6L-9OI130_assertion
;
np:hasProvenance
dgn-np:NP438839.RA645r-53oUn3Ttu0uJ8U506D8vFcxpohoZxtTB6L-9OI130_provenance
;
np:hasPublicationInfo
dgn-np:NP438839.RA645r-53oUn3Ttu0uJ8U506D8vFcxpohoZxtTB6L-9OI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP438839.RA645r-53oUn3Ttu0uJ8U506D8vFcxpohoZxtTB6L-9OI130_assertion
a
np:Assertion
.
dgn-np:NP438839.RA645r-53oUn3Ttu0uJ8U506D8vFcxpohoZxtTB6L-9OI130_provenance
a
np:Provenance
.
dgn-np:NP438839.RA645r-53oUn3Ttu0uJ8U506D8vFcxpohoZxtTB6L-9OI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP438839.RA645r-53oUn3Ttu0uJ8U506D8vFcxpohoZxtTB6L-9OI130_assertion
{
miriam-gene:7145
a
ncit:C16612
.
lld:C0025202
a
ncit:C7057
.
dgn-gda:DGN71cd1886086e16a4e7982f401c135ff5
sio:SIO_000628
miriam-gene:7145
,
lld:C0025202
;
a
sio:SIO_001121
.
}
dgn-np:NP438839.RA645r-53oUn3Ttu0uJ8U506D8vFcxpohoZxtTB6L-9OI130_provenance
{
dgn-np:NP438839.RA645r-53oUn3Ttu0uJ8U506D8vFcxpohoZxtTB6L-9OI130_assertion
dcterms:description
"[The phosphatase and tensin homologue deleted from chromosome 10 (PTEN) is one of the genes on chromosome 10 whose of which the loss or inactivation may play an important role in melanoma tumorigenesis, but functional studies directly demonstrating PTEN involvement in melanomas are necessary to confirm this role.]. 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:12782594
;
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:NP438839.RA645r-53oUn3Ttu0uJ8U506D8vFcxpohoZxtTB6L-9OI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:19+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" .
}