@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4
> .
@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:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_head
{
this:
np:hasAssertion
dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_assertion
;
np:hasProvenance
dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_provenance
;
np:hasPublicationInfo
dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_assertion
a
np:Assertion
.
dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_provenance
a
np:Provenance
.
dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_assertion
{
miriam-gene:2316
a
ncit:C16612
.
lld:C0266464
a
ncit:C7057
.
dgn-gda:DGN8baa2b76e4eb829b23959b1e78e09716
sio:SIO_000628
miriam-gene:2316
,
lld:C0266464
;
a
sio:SIO_001121
.
}
dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_provenance
{
dgn-np:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_assertion
dcterms:description
"[We identified 30 patients as having both PNH and PMG on brain imaging, reviewed clinical data and brain imaging studies (or neuropathology summary) for all, and performed mutation analysis of FLNA in nine 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:16311271
;
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:NP672155.RACqWbYpuLE9LsYV2fROETy9wsdHuwzkNXfvvYUAY6no4130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:45+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" .
}