@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP545703.RAcRWiWW6PvnpXhkyIdDW8p2zaTRBGuClqE5PxQzmGtww
> .
@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:NP545703.RAcRWiWW6PvnpXhkyIdDW8p2zaTRBGuClqE5PxQzmGtww130_head
{
this:
np:hasAssertion
dgn-np:NP545703.RAcRWiWW6PvnpXhkyIdDW8p2zaTRBGuClqE5PxQzmGtww130_assertion
;
np:hasProvenance
dgn-np:NP545703.RAcRWiWW6PvnpXhkyIdDW8p2zaTRBGuClqE5PxQzmGtww130_provenance
;
np:hasPublicationInfo
dgn-np:NP545703.RAcRWiWW6PvnpXhkyIdDW8p2zaTRBGuClqE5PxQzmGtww130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP545703.RAcRWiWW6PvnpXhkyIdDW8p2zaTRBGuClqE5PxQzmGtww130_assertion
a
np:Assertion
.
dgn-np:NP545703.RAcRWiWW6PvnpXhkyIdDW8p2zaTRBGuClqE5PxQzmGtww130_provenance
a
np:Provenance
.
dgn-np:NP545703.RAcRWiWW6PvnpXhkyIdDW8p2zaTRBGuClqE5PxQzmGtww130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP545703.RAcRWiWW6PvnpXhkyIdDW8p2zaTRBGuClqE5PxQzmGtww130_assertion
{
miriam-gene:27034
a
ncit:C16612
.
lld:C0022104
a
ncit:C7057
.
dgn-gda:DGN81a6d312826435a2ddffb52252112b7d
sio:SIO_000628
miriam-gene:27034
,
lld:C0022104
;
a
sio:SIO_001121
.
}
dgn-np:NP545703.RAcRWiWW6PvnpXhkyIdDW8p2zaTRBGuClqE5PxQzmGtww130_provenance
{
dgn-np:NP545703.RAcRWiWW6PvnpXhkyIdDW8p2zaTRBGuClqE5PxQzmGtww130_assertion
dcterms:description
"[Therefore we applied the Combinatorial Mismatch Scanning (CMS) method that compares identity by state (IBS) (under the presumption of identity by descent (IBD)) sharing in distantly related individuals from such populations where standard linkage and association analyses are difficult to implement.]. 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:16515697
;
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:NP545703.RAcRWiWW6PvnpXhkyIdDW8p2zaTRBGuClqE5PxQzmGtww130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:37:29+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" .
}