@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP828066.RAyn0S6FQrT8I9p_g1d9xufyUMQCvKeJZgYsGnjp_Mflo
> .
@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:NP828066.RAyn0S6FQrT8I9p_g1d9xufyUMQCvKeJZgYsGnjp_Mflo130_head
{
this:
np:hasAssertion
dgn-np:NP828066.RAyn0S6FQrT8I9p_g1d9xufyUMQCvKeJZgYsGnjp_Mflo130_assertion
;
np:hasProvenance
dgn-np:NP828066.RAyn0S6FQrT8I9p_g1d9xufyUMQCvKeJZgYsGnjp_Mflo130_provenance
;
np:hasPublicationInfo
dgn-np:NP828066.RAyn0S6FQrT8I9p_g1d9xufyUMQCvKeJZgYsGnjp_Mflo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP828066.RAyn0S6FQrT8I9p_g1d9xufyUMQCvKeJZgYsGnjp_Mflo130_assertion
a
np:Assertion
.
dgn-np:NP828066.RAyn0S6FQrT8I9p_g1d9xufyUMQCvKeJZgYsGnjp_Mflo130_provenance
a
np:Provenance
.
dgn-np:NP828066.RAyn0S6FQrT8I9p_g1d9xufyUMQCvKeJZgYsGnjp_Mflo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP828066.RAyn0S6FQrT8I9p_g1d9xufyUMQCvKeJZgYsGnjp_Mflo130_assertion
{
miriam-gene:94
a
ncit:C16612
.
lld:C0158570
a
ncit:C7057
.
dgn-gda:DGN0a8cec3680cb0123c1c900427bcaa11e
sio:SIO_000628
miriam-gene:94
,
lld:C0158570
;
a
sio:SIO_001121
.
}
dgn-np:NP828066.RAyn0S6FQrT8I9p_g1d9xufyUMQCvKeJZgYsGnjp_Mflo130_provenance
{
dgn-np:NP828066.RAyn0S6FQrT8I9p_g1d9xufyUMQCvKeJZgYsGnjp_Mflo130_assertion
dcterms:description
"[The pathogenesis regarding heterogeneity of vascular malformations in patients with HHT has been obscure, although it has become possible to partially explain the pathogenesis from the identification of two distinct genes, endoglin and ALK-1.]. 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:11019486
;
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:NP828066.RAyn0S6FQrT8I9p_g1d9xufyUMQCvKeJZgYsGnjp_Mflo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:40:27+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" .
}