@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP459906.RAXZatbxXYO-ZJHbkK6sjLq87iKpm5R1wywKpI7uxq54k
> .
@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:NP459906.RAXZatbxXYO-ZJHbkK6sjLq87iKpm5R1wywKpI7uxq54k130_head
{
this:
np:hasAssertion
dgn-np:NP459906.RAXZatbxXYO-ZJHbkK6sjLq87iKpm5R1wywKpI7uxq54k130_assertion
;
np:hasProvenance
dgn-np:NP459906.RAXZatbxXYO-ZJHbkK6sjLq87iKpm5R1wywKpI7uxq54k130_provenance
;
np:hasPublicationInfo
dgn-np:NP459906.RAXZatbxXYO-ZJHbkK6sjLq87iKpm5R1wywKpI7uxq54k130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP459906.RAXZatbxXYO-ZJHbkK6sjLq87iKpm5R1wywKpI7uxq54k130_assertion
a
np:Assertion
.
dgn-np:NP459906.RAXZatbxXYO-ZJHbkK6sjLq87iKpm5R1wywKpI7uxq54k130_provenance
a
np:Provenance
.
dgn-np:NP459906.RAXZatbxXYO-ZJHbkK6sjLq87iKpm5R1wywKpI7uxq54k130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP459906.RAXZatbxXYO-ZJHbkK6sjLq87iKpm5R1wywKpI7uxq54k130_assertion
{
miriam-gene:4000
a
ncit:C16612
.
lld:C0231341
a
ncit:C7057
.
dgn-gda:DGNc15b0bdb53670d3406041be15d55e12a
sio:SIO_000628
miriam-gene:4000
,
lld:C0231341
;
a
sio:SIO_001121
.
}
dgn-np:NP459906.RAXZatbxXYO-ZJHbkK6sjLq87iKpm5R1wywKpI7uxq54k130_provenance
{
dgn-np:NP459906.RAXZatbxXYO-ZJHbkK6sjLq87iKpm5R1wywKpI7uxq54k130_assertion
dcterms:description
"[Advances in molecular genetics of apparently unrelated disorders, involving muscle, heart, nerve, fat, bone, liver, skin tissues and premature ageing, have enriched our knowledge of the diverse phenotypes associated with lamin A/C mutations.]. 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:15367859
;
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:NP459906.RAXZatbxXYO-ZJHbkK6sjLq87iKpm5R1wywKpI7uxq54k130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:45:13+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" .
}