@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP840044.RAIlEYdkP9n16YH61if8neljzgf_x4ldj_IUzdKA-ocSU
> .
@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:NP840044.RAIlEYdkP9n16YH61if8neljzgf_x4ldj_IUzdKA-ocSU130_head
{
this:
np:hasAssertion
dgn-np:NP840044.RAIlEYdkP9n16YH61if8neljzgf_x4ldj_IUzdKA-ocSU130_assertion
;
np:hasProvenance
dgn-np:NP840044.RAIlEYdkP9n16YH61if8neljzgf_x4ldj_IUzdKA-ocSU130_provenance
;
np:hasPublicationInfo
dgn-np:NP840044.RAIlEYdkP9n16YH61if8neljzgf_x4ldj_IUzdKA-ocSU130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP840044.RAIlEYdkP9n16YH61if8neljzgf_x4ldj_IUzdKA-ocSU130_assertion
a
np:Assertion
.
dgn-np:NP840044.RAIlEYdkP9n16YH61if8neljzgf_x4ldj_IUzdKA-ocSU130_provenance
a
np:Provenance
.
dgn-np:NP840044.RAIlEYdkP9n16YH61if8neljzgf_x4ldj_IUzdKA-ocSU130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP840044.RAIlEYdkP9n16YH61if8neljzgf_x4ldj_IUzdKA-ocSU130_assertion
{
miriam-gene:5290
a
ncit:C16612
.
lld:C0220668
a
ncit:C7057
.
dgn-gda:DGN3ec5ff37a0b8d8a0e2bfdc0abf9df194
sio:SIO_000628
miriam-gene:5290
,
lld:C0220668
;
a
sio:SIO_001121
.
}
dgn-np:NP840044.RAIlEYdkP9n16YH61if8neljzgf_x4ldj_IUzdKA-ocSU130_provenance
{
dgn-np:NP840044.RAIlEYdkP9n16YH61if8neljzgf_x4ldj_IUzdKA-ocSU130_assertion
dcterms:description
"[These findings provide evidence that mutations of the PIK3CA gene occur in the putative precursor lesions of CCA, strongly suggesting that they are very early events in tumourigenesis, probably initiating the malignant transformation of endometriosis.]. 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:21735444
;
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:NP840044.RAIlEYdkP9n16YH61if8neljzgf_x4ldj_IUzdKA-ocSU130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:33+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" .
}