@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP564961.RABZsIExAcCmDVrAOd51fTT4Kyb_wkYZ7d4ancqAhGoQo
> .
@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:NP564961.RABZsIExAcCmDVrAOd51fTT4Kyb_wkYZ7d4ancqAhGoQo130_head
{
this:
np:hasAssertion
dgn-np:NP564961.RABZsIExAcCmDVrAOd51fTT4Kyb_wkYZ7d4ancqAhGoQo130_assertion
;
np:hasProvenance
dgn-np:NP564961.RABZsIExAcCmDVrAOd51fTT4Kyb_wkYZ7d4ancqAhGoQo130_provenance
;
np:hasPublicationInfo
dgn-np:NP564961.RABZsIExAcCmDVrAOd51fTT4Kyb_wkYZ7d4ancqAhGoQo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP564961.RABZsIExAcCmDVrAOd51fTT4Kyb_wkYZ7d4ancqAhGoQo130_assertion
a
np:Assertion
.
dgn-np:NP564961.RABZsIExAcCmDVrAOd51fTT4Kyb_wkYZ7d4ancqAhGoQo130_provenance
a
np:Provenance
.
dgn-np:NP564961.RABZsIExAcCmDVrAOd51fTT4Kyb_wkYZ7d4ancqAhGoQo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP564961.RABZsIExAcCmDVrAOd51fTT4Kyb_wkYZ7d4ancqAhGoQo130_assertion
{
miriam-gene:10383
a
ncit:C16612
.
lld:C0272187
a
ncit:C7057
.
dgn-gda:DGNb97ed75bdcecbdf0ec3586bee0fd9611
sio:SIO_000628
miriam-gene:10383
,
lld:C0272187
;
a
sio:SIO_001121
.
}
dgn-np:NP564961.RABZsIExAcCmDVrAOd51fTT4Kyb_wkYZ7d4ancqAhGoQo130_provenance
{
dgn-np:NP564961.RABZsIExAcCmDVrAOd51fTT4Kyb_wkYZ7d4ancqAhGoQo130_assertion
dcterms:description
"[The aim of this study was to analyze mutations in DNA from patients with leukocyte adhesion deficiency (LAD), an immunodeficiency caused by absence of the beta(2) subunit (CD18) of the leukocyte integrins LFA-1 (CD11a/CD18), Mac-1 (CD11b/CD18), p150,95 (CD11c/CD18), and CR4 (CD11d/CD18).]. 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:11882363
;
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:NP564961.RABZsIExAcCmDVrAOd51fTT4Kyb_wkYZ7d4ancqAhGoQo130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:40+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" .
}