@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0
> .
@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:NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_head
{
this:
np:hasAssertion
dgn-np:NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_assertion
;
np:hasProvenance
dgn-np:NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_provenance
;
np:hasPublicationInfo
dgn-np:NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_assertion
a
np:Assertion
.
dgn-np:NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_provenance
a
np:Provenance
.
dgn-np:NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_assertion
{
miriam-gene:94
a
ncit:C16612
.
lld:C0039445
a
ncit:C7057
.
dgn-gda:DGN93886070641de2c6c8e1a8dbea716120
sio:SIO_000628
miriam-gene:94
,
lld:C0039445
;
a
sio:SIO_001122
.
}
dgn-np:NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_provenance
{
dgn-np:NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_assertion
dcterms:description
"[A questionnaire based study provides evidence that the hereditary hemorrhagic telangiectasia (HHT) phenotype caused by mutations in endoglin (HHT1) is distinct from, and more severe than, HHT caused by mutations in ALK1 (HHT2).]. 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:12920067
;
prov:wasDerivedFrom
dgn-void:lhgdn-20090331
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:lhgdn-20090331
pav:importedOn
"2009-03-31"^^
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:NP201046.RAw68XeYJ7OzoinVXgTTqrpPnEdBI1IUtOIpT4v0bXuM0130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:43:18+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" .
}