@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI
> .
@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:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_head
{
this:
np:hasAssertion
dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_assertion
;
np:hasProvenance
dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_provenance
;
np:hasPublicationInfo
dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_assertion
a
np:Assertion
.
dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_provenance
a
np:Provenance
.
dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_assertion
{
miriam-gene:727
a
ncit:C16612
.
lld:C0343713
a
ncit:C7057
.
dgn-gda:DGNd0af05045f3b4048ce95bee172b31a70
sio:SIO_000628
miriam-gene:727
,
lld:C0343713
;
a
sio:SIO_001121
.
}
dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_provenance
{
dgn-np:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_assertion
dcterms:description
"[Absence of the fifth component of complement (C5) by immunochemical assay and marked deficiency by hemolytic assay (less than 0.1%) was found in a family in which the oldest male child had suffered severe and recurrent meningococcemia at age 15 years, two brothers developed meningococcal meningitis four years later (at ages 18 and 14 years), and a sister had the gonococcal arthritis-dermatitis syndrome.]. 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:6785713
;
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:NP245629.RABgQic-PY2fhN_moK4H5aKID31siC3pfSstk2rOh3gnI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:17+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" .
}