@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP885657.RAIndvUAcH6a7oECUBrZ2u2MJqh7JOr-wWaGMt7GBHRPs
> .
@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:NP885657.RAIndvUAcH6a7oECUBrZ2u2MJqh7JOr-wWaGMt7GBHRPs130_head
{
this:
np:hasAssertion
dgn-np:NP885657.RAIndvUAcH6a7oECUBrZ2u2MJqh7JOr-wWaGMt7GBHRPs130_assertion
;
np:hasProvenance
dgn-np:NP885657.RAIndvUAcH6a7oECUBrZ2u2MJqh7JOr-wWaGMt7GBHRPs130_provenance
;
np:hasPublicationInfo
dgn-np:NP885657.RAIndvUAcH6a7oECUBrZ2u2MJqh7JOr-wWaGMt7GBHRPs130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP885657.RAIndvUAcH6a7oECUBrZ2u2MJqh7JOr-wWaGMt7GBHRPs130_assertion
a
np:Assertion
.
dgn-np:NP885657.RAIndvUAcH6a7oECUBrZ2u2MJqh7JOr-wWaGMt7GBHRPs130_provenance
a
np:Provenance
.
dgn-np:NP885657.RAIndvUAcH6a7oECUBrZ2u2MJqh7JOr-wWaGMt7GBHRPs130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP885657.RAIndvUAcH6a7oECUBrZ2u2MJqh7JOr-wWaGMt7GBHRPs130_assertion
{
miriam-gene:4089
a
ncit:C16612
.
lld:C0003857
a
ncit:C7057
.
dgn-gda:DGNa4c996840d2c6f22976c3c31e59f27ab
sio:SIO_000628
miriam-gene:4089
,
lld:C0003857
;
a
sio:SIO_001121
.
}
dgn-np:NP885657.RAIndvUAcH6a7oECUBrZ2u2MJqh7JOr-wWaGMt7GBHRPs130_provenance
{
dgn-np:NP885657.RAIndvUAcH6a7oECUBrZ2u2MJqh7JOr-wWaGMt7GBHRPs130_assertion
dcterms:description
"[Patients with juvenile polyposis who have an MADH4 mutation should be screened for the vascular lesions associated with hereditary haemorrhagic telangiectasia, especially occult arteriovenous malformations in visceral organs that may otherwise present suddenly with serious medical consequences.]. 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:15031030
;
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:NP885657.RAIndvUAcH6a7oECUBrZ2u2MJqh7JOr-wWaGMt7GBHRPs130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:41:01+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" .
}