@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM
> .
@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:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_head
{
this:
np:hasAssertion
dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_assertion
;
np:hasProvenance
dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_provenance
;
np:hasPublicationInfo
dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_assertion
a
np:Assertion
.
dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_provenance
a
np:Provenance
.
dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_assertion
{
miriam-gene:7139
a
ncit:C16612
.
lld:C1449563
a
ncit:C7057
.
dgn-gda:DGN31d8356918f45a8469f364ce1d6e76bc
sio:SIO_000628
miriam-gene:7139
,
lld:C1449563
;
a
sio:SIO_001121
.
}
dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_provenance
{
dgn-np:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_assertion
dcterms:description
"[Known candidate loci for isolated conduction disorders, isolated DCM and conduction disorders complicated by DCM were excluded from disease causation in this family by linkage analysis, with the exception of the DCM-associated (CMD1D) locus on chromosome 1q32, where a maximum multipoint lod score of 3.7 in the interval between D1S3753 and D1S414, was generated.]. 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:16086176
;
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:NP301206.RABNTUw2T_-fB8KF1HPE_eHQx3TVYJC33suwBXQNzIkZM130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:51+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" .
}