@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP669013.RADdQ3x53tAq1ZvBkWt_f41MBMNEs1VH-PgyBPqNnG5qk
> .
@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:NP669013.RADdQ3x53tAq1ZvBkWt_f41MBMNEs1VH-PgyBPqNnG5qk130_head
{
this:
np:hasAssertion
dgn-np:NP669013.RADdQ3x53tAq1ZvBkWt_f41MBMNEs1VH-PgyBPqNnG5qk130_assertion
;
np:hasProvenance
dgn-np:NP669013.RADdQ3x53tAq1ZvBkWt_f41MBMNEs1VH-PgyBPqNnG5qk130_provenance
;
np:hasPublicationInfo
dgn-np:NP669013.RADdQ3x53tAq1ZvBkWt_f41MBMNEs1VH-PgyBPqNnG5qk130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP669013.RADdQ3x53tAq1ZvBkWt_f41MBMNEs1VH-PgyBPqNnG5qk130_assertion
a
np:Assertion
.
dgn-np:NP669013.RADdQ3x53tAq1ZvBkWt_f41MBMNEs1VH-PgyBPqNnG5qk130_provenance
a
np:Provenance
.
dgn-np:NP669013.RADdQ3x53tAq1ZvBkWt_f41MBMNEs1VH-PgyBPqNnG5qk130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP669013.RADdQ3x53tAq1ZvBkWt_f41MBMNEs1VH-PgyBPqNnG5qk130_assertion
{
miriam-gene:6288
a
ncit:C16612
.
lld:C0031069
a
ncit:C7057
.
dgn-gda:DGN4cd60123b014c2d1d15fd962de2c1696
sio:SIO_000628
miriam-gene:6288
,
lld:C0031069
;
a
sio:SIO_001121
.
}
dgn-np:NP669013.RADdQ3x53tAq1ZvBkWt_f41MBMNEs1VH-PgyBPqNnG5qk130_provenance
{
dgn-np:NP669013.RADdQ3x53tAq1ZvBkWt_f41MBMNEs1VH-PgyBPqNnG5qk130_assertion
dcterms:description
"[This study, which provides new insights into the role of SAA1 in the pathophysiology of FMF, represents the first example of deviations from HWE and selection involving the modifier gene of a Mendelian disorder.]. 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:19888326
;
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:NP669013.RADdQ3x53tAq1ZvBkWt_f41MBMNEs1VH-PgyBPqNnG5qk130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:38:44+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" .
}