@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP773403.RA8cl1h-WwlxLxdCx-1FaMP-gLoNiMArg2XoSznGnnLAI
> .
@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:NP773403.RA8cl1h-WwlxLxdCx-1FaMP-gLoNiMArg2XoSznGnnLAI130_head
{
this:
np:hasAssertion
dgn-np:NP773403.RA8cl1h-WwlxLxdCx-1FaMP-gLoNiMArg2XoSznGnnLAI130_assertion
;
np:hasProvenance
dgn-np:NP773403.RA8cl1h-WwlxLxdCx-1FaMP-gLoNiMArg2XoSznGnnLAI130_provenance
;
np:hasPublicationInfo
dgn-np:NP773403.RA8cl1h-WwlxLxdCx-1FaMP-gLoNiMArg2XoSznGnnLAI130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP773403.RA8cl1h-WwlxLxdCx-1FaMP-gLoNiMArg2XoSznGnnLAI130_assertion
a
np:Assertion
.
dgn-np:NP773403.RA8cl1h-WwlxLxdCx-1FaMP-gLoNiMArg2XoSznGnnLAI130_provenance
a
np:Provenance
.
dgn-np:NP773403.RA8cl1h-WwlxLxdCx-1FaMP-gLoNiMArg2XoSznGnnLAI130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP773403.RA8cl1h-WwlxLxdCx-1FaMP-gLoNiMArg2XoSznGnnLAI130_assertion
{
miriam-gene:57190
a
ncit:C16612
.
lld:C0270962
a
ncit:C7057
.
dgn-gda:DGN361334105607177b0eb13cd2a7fc3e28
sio:SIO_000628
miriam-gene:57190
,
lld:C0270962
;
a
sio:SIO_001121
.
}
dgn-np:NP773403.RA8cl1h-WwlxLxdCx-1FaMP-gLoNiMArg2XoSznGnnLAI130_provenance
{
dgn-np:NP773403.RA8cl1h-WwlxLxdCx-1FaMP-gLoNiMArg2XoSznGnnLAI130_assertion
dcterms:description
"[To report a family in which congenital fibre type disproportion (CFTD) and minicore disease have been observed in members of the same family, and raise the question of the relationship between CFTD and minicores.]. 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:7669390
;
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:NP773403.RA8cl1h-WwlxLxdCx-1FaMP-gLoNiMArg2XoSznGnnLAI130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:48+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" .
}