@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1105278.RAGGBUQVcJ4n96c3Z35kRHiX0UhmRjdeuHwc7Xhul7Z7c
> .
@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/
> .
@prefix wi: <
http://purl.org/ontology/wi/core#
> .
@prefix prov: <
http://www.w3.org/ns/prov#
> .
@prefix pav: <
http://purl.org/pav/
> .
@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/resource/nanopub/
> .
@prefix dgn-gda: <
http://rdf.disgenet.org/resource/gda/
> .
@prefix dgn-void: <
http://rdf.disgenet.org/v4.0.0/void/
> .
dgn-np:NP1105278.RAGGBUQVcJ4n96c3Z35kRHiX0UhmRjdeuHwc7Xhul7Z7c130_head
{
this:
np:hasAssertion
dgn-np:NP1105278.RAGGBUQVcJ4n96c3Z35kRHiX0UhmRjdeuHwc7Xhul7Z7c130_assertion
;
np:hasProvenance
dgn-np:NP1105278.RAGGBUQVcJ4n96c3Z35kRHiX0UhmRjdeuHwc7Xhul7Z7c130_provenance
;
np:hasPublicationInfo
dgn-np:NP1105278.RAGGBUQVcJ4n96c3Z35kRHiX0UhmRjdeuHwc7Xhul7Z7c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1105278.RAGGBUQVcJ4n96c3Z35kRHiX0UhmRjdeuHwc7Xhul7Z7c130_assertion
a
np:Assertion
.
dgn-np:NP1105278.RAGGBUQVcJ4n96c3Z35kRHiX0UhmRjdeuHwc7Xhul7Z7c130_provenance
a
np:Provenance
.
dgn-np:NP1105278.RAGGBUQVcJ4n96c3Z35kRHiX0UhmRjdeuHwc7Xhul7Z7c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1105278.RAGGBUQVcJ4n96c3Z35kRHiX0UhmRjdeuHwc7Xhul7Z7c130_assertion
{
miriam-gene:4534
a
ncit:C16612
.
lld:C0175709
a
ncit:C7057
.
dgn-gda:DGN734b041f1913f5f441baef2f36979440
sio:SIO_000628
miriam-gene:4534
,
lld:C0175709
;
a
sio:SIO_001121
.
}
dgn-np:NP1105278.RAGGBUQVcJ4n96c3Z35kRHiX0UhmRjdeuHwc7Xhul7Z7c130_provenance
{
dgn-np:NP1105278.RAGGBUQVcJ4n96c3Z35kRHiX0UhmRjdeuHwc7Xhul7Z7c130_assertion
dcterms:description
"[This study expands the phenotypic spectrum associated with TTN mutations and indicates that TTN mutation analysis should be considered in cases of possible CNM without mutations in the classic CNM genes.]. 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:23975875
;
prov:wasDerivedFrom
dgn-void:befree-2016
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-2016
pav:importedOn
"2016-02-19"^^
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:NP1105278.RAGGBUQVcJ4n96c3Z35kRHiX0UhmRjdeuHwc7Xhul7Z7c130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:50:07+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:disgenetv3.0rdf
;
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
"v4.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v4.0.0" .
}