@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP727429.RANlF_P54vX1AB0pe1071WNHqwf2eSIhjoVwz16q_4U5Q
> .
@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:NP727429.RANlF_P54vX1AB0pe1071WNHqwf2eSIhjoVwz16q_4U5Q130_head
{
this:
np:hasAssertion
dgn-np:NP727429.RANlF_P54vX1AB0pe1071WNHqwf2eSIhjoVwz16q_4U5Q130_assertion
;
np:hasProvenance
dgn-np:NP727429.RANlF_P54vX1AB0pe1071WNHqwf2eSIhjoVwz16q_4U5Q130_provenance
;
np:hasPublicationInfo
dgn-np:NP727429.RANlF_P54vX1AB0pe1071WNHqwf2eSIhjoVwz16q_4U5Q130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP727429.RANlF_P54vX1AB0pe1071WNHqwf2eSIhjoVwz16q_4U5Q130_assertion
a
np:Assertion
.
dgn-np:NP727429.RANlF_P54vX1AB0pe1071WNHqwf2eSIhjoVwz16q_4U5Q130_provenance
a
np:Provenance
.
dgn-np:NP727429.RANlF_P54vX1AB0pe1071WNHqwf2eSIhjoVwz16q_4U5Q130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP727429.RANlF_P54vX1AB0pe1071WNHqwf2eSIhjoVwz16q_4U5Q130_assertion
{
miriam-gene:3075
a
ncit:C16612
.
lld:C2717961
a
ncit:C7057
.
dgn-gda:DGNe343e8cfd1dde809e13413c44fdfc91d
sio:SIO_000628
miriam-gene:3075
,
lld:C2717961
;
a
sio:SIO_001121
.
}
dgn-np:NP727429.RANlF_P54vX1AB0pe1071WNHqwf2eSIhjoVwz16q_4U5Q130_provenance
{
dgn-np:NP727429.RANlF_P54vX1AB0pe1071WNHqwf2eSIhjoVwz16q_4U5Q130_assertion
dcterms:description
"[Diarrhea-negative HUS is associated with complement dysregulation in up to 50% of cases, caused by mutations in complement factor H, membrane cofactor protein, factor I or factor B, or by autoantibodies against factor H. The incomplete penetrance of mutations in either ADAMTS13 or complement regulatory genes suggests that precipitating events or triggers may be required to cause thrombotic microangiopathy in many patients.]. 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:18215115
;
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:NP727429.RANlF_P54vX1AB0pe1071WNHqwf2eSIhjoVwz16q_4U5Q130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:21+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" .
}