@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP589840.RA6LV0FJb3cEzJviawAvd56Mi0iYHebKPpGwmslFNUiiA
> .
@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:NP589840.RA6LV0FJb3cEzJviawAvd56Mi0iYHebKPpGwmslFNUiiA130_head
{
this:
np:hasAssertion
dgn-np:NP589840.RA6LV0FJb3cEzJviawAvd56Mi0iYHebKPpGwmslFNUiiA130_assertion
;
np:hasProvenance
dgn-np:NP589840.RA6LV0FJb3cEzJviawAvd56Mi0iYHebKPpGwmslFNUiiA130_provenance
;
np:hasPublicationInfo
dgn-np:NP589840.RA6LV0FJb3cEzJviawAvd56Mi0iYHebKPpGwmslFNUiiA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP589840.RA6LV0FJb3cEzJviawAvd56Mi0iYHebKPpGwmslFNUiiA130_assertion
a
np:Assertion
.
dgn-np:NP589840.RA6LV0FJb3cEzJviawAvd56Mi0iYHebKPpGwmslFNUiiA130_provenance
a
np:Provenance
.
dgn-np:NP589840.RA6LV0FJb3cEzJviawAvd56Mi0iYHebKPpGwmslFNUiiA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP589840.RA6LV0FJb3cEzJviawAvd56Mi0iYHebKPpGwmslFNUiiA130_assertion
{
miriam-gene:324
a
ncit:C16612
.
lld:C0032580
a
ncit:C7057
.
dgn-gda:DGNeecc9723c24ca39c3bd3f7d897ccd6ce
sio:SIO_000628
miriam-gene:324
,
lld:C0032580
;
a
sio:SIO_001121
.
}
dgn-np:NP589840.RA6LV0FJb3cEzJviawAvd56Mi0iYHebKPpGwmslFNUiiA130_provenance
{
dgn-np:NP589840.RA6LV0FJb3cEzJviawAvd56Mi0iYHebKPpGwmslFNUiiA130_assertion
dcterms:description
"[In patients with FAP and identifiable APC gene mutation, CNS tumors, especially medulloblastoma which developed in most cases during childhood, are more common in females with FAP and APC gene mutation in codons 686-1217.]. 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:17238184
;
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:NP589840.RA6LV0FJb3cEzJviawAvd56Mi0iYHebKPpGwmslFNUiiA130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:46:12+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" .
}