@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM
> .
@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:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_head
{
this:
np:hasAssertion
dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_assertion
;
np:hasProvenance
dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_provenance
;
np:hasPublicationInfo
dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_assertion
a
np:Assertion
.
dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_provenance
a
np:Provenance
.
dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_assertion
{
miriam-gene:657
a
ncit:C16612
.
lld:C0032584
a
ncit:C7057
.
dgn-gda:DGN40ebe3c8fc4106362326899c8b78d620
sio:SIO_000628
miriam-gene:657
,
lld:C0032584
;
a
sio:SIO_001121
.
}
dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_provenance
{
dgn-np:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_assertion
dcterms:description
"[If patients present with mixed morphology polyps in the large bowel that are autosomal dominantly inherited and corresponding absence of upper gastrointestinal abnormalities, the gene to begin mutation screening should be BMPR1A rather than APC.]. 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:19773747
;
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:NP764880.RAselh0VORtpjOmpJzPeYDxVOfLv2switRh8pEVM0HnOM130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:47:31+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" .
}