@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo
> .
@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:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_head
{
this:
np:hasAssertion
dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_assertion
;
np:hasProvenance
dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_provenance
;
np:hasPublicationInfo
dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_assertion
a
np:Assertion
.
dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_provenance
a
np:Provenance
.
dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_assertion
{
miriam-gene:11122
a
ncit:C16612
.
lld:C0006826
a
ncit:C7057
.
dgn-gda:DGN8107dd1784f323fc695e98164f50bd06
sio:SIO_000628
miriam-gene:11122
,
lld:C0006826
;
a
sio:SIO_001121
.
}
dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_provenance
{
dgn-np:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_assertion
dcterms:description
"[Contrary to the previous report on the frequent PTPTR phosphatase domain mutations in colon cancers, this study demonstrated that the somatic mutation of the PTPRT phosphatase domain rarely occurred in common human cancers.]. 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:17223850
;
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:NP262679.RAOmDvOzX0Jzvoeq2jUyyf64XNkzvY-Qc1MWIz6lbmSjo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:26+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" .
}