@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP476381.RASh2ihMYJ9rycrl1WYBOYgpC7fYirmhgEFFORn5pZELA
> .
@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:NP476381.RASh2ihMYJ9rycrl1WYBOYgpC7fYirmhgEFFORn5pZELA130_head
{
this:
np:hasAssertion
dgn-np:NP476381.RASh2ihMYJ9rycrl1WYBOYgpC7fYirmhgEFFORn5pZELA130_assertion
;
np:hasProvenance
dgn-np:NP476381.RASh2ihMYJ9rycrl1WYBOYgpC7fYirmhgEFFORn5pZELA130_provenance
;
np:hasPublicationInfo
dgn-np:NP476381.RASh2ihMYJ9rycrl1WYBOYgpC7fYirmhgEFFORn5pZELA130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP476381.RASh2ihMYJ9rycrl1WYBOYgpC7fYirmhgEFFORn5pZELA130_assertion
a
np:Assertion
.
dgn-np:NP476381.RASh2ihMYJ9rycrl1WYBOYgpC7fYirmhgEFFORn5pZELA130_provenance
a
np:Provenance
.
dgn-np:NP476381.RASh2ihMYJ9rycrl1WYBOYgpC7fYirmhgEFFORn5pZELA130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP476381.RASh2ihMYJ9rycrl1WYBOYgpC7fYirmhgEFFORn5pZELA130_assertion
{
miriam-gene:2022
a
ncit:C16612
.
lld:C0917804
a
ncit:C7057
.
dgn-gda:DGNaaaa501ec055884ae5f1fd2973d54e74
sio:SIO_000628
miriam-gene:2022
,
lld:C0917804
;
a
sio:SIO_001121
.
}
dgn-np:NP476381.RASh2ihMYJ9rycrl1WYBOYgpC7fYirmhgEFFORn5pZELA130_provenance
{
dgn-np:NP476381.RASh2ihMYJ9rycrl1WYBOYgpC7fYirmhgEFFORn5pZELA130_assertion
dcterms:description
"[Our data confirm that endoglin levels correlate with the presence or absence of mutation in HHT1 families, allowing the early identification of affected newborns that should be screened clinically to avoid serious complications of this disorder, such as cerebral arteriovenous malformations.]. 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:10625079
;
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:NP476381.RASh2ihMYJ9rycrl1WYBOYgpC7fYirmhgEFFORn5pZELA130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:45+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" .
}