@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP590664.RAJCdP3zVgcBrK9P0JJGKH4CuSydPxygo3uFa9tU5krrg
> .
@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:NP590664.RAJCdP3zVgcBrK9P0JJGKH4CuSydPxygo3uFa9tU5krrg130_head
{
this:
np:hasAssertion
dgn-np:NP590664.RAJCdP3zVgcBrK9P0JJGKH4CuSydPxygo3uFa9tU5krrg130_assertion
;
np:hasProvenance
dgn-np:NP590664.RAJCdP3zVgcBrK9P0JJGKH4CuSydPxygo3uFa9tU5krrg130_provenance
;
np:hasPublicationInfo
dgn-np:NP590664.RAJCdP3zVgcBrK9P0JJGKH4CuSydPxygo3uFa9tU5krrg130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP590664.RAJCdP3zVgcBrK9P0JJGKH4CuSydPxygo3uFa9tU5krrg130_assertion
a
np:Assertion
.
dgn-np:NP590664.RAJCdP3zVgcBrK9P0JJGKH4CuSydPxygo3uFa9tU5krrg130_provenance
a
np:Provenance
.
dgn-np:NP590664.RAJCdP3zVgcBrK9P0JJGKH4CuSydPxygo3uFa9tU5krrg130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP590664.RAJCdP3zVgcBrK9P0JJGKH4CuSydPxygo3uFa9tU5krrg130_assertion
{
miriam-gene:2316
a
ncit:C16612
.
lld:C0024790
a
ncit:C7057
.
dgn-gda:DGNc8587276d229dad30836f7723e8ba456
sio:SIO_000628
miriam-gene:2316
,
lld:C0024790
;
a
sio:SIO_001121
.
}
dgn-np:NP590664.RAJCdP3zVgcBrK9P0JJGKH4CuSydPxygo3uFa9tU5krrg130_provenance
{
dgn-np:NP590664.RAJCdP3zVgcBrK9P0JJGKH4CuSydPxygo3uFa9tU5krrg130_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:NP590664.RAJCdP3zVgcBrK9P0JJGKH4CuSydPxygo3uFa9tU5krrg130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:55+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" .
}