@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP44185.RA4rmJPwPgvDfv8nixoQtkZ8xQjIoJpFS9NQ_s4hV2SG0
> .
@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:NP44185.RA4rmJPwPgvDfv8nixoQtkZ8xQjIoJpFS9NQ_s4hV2SG0130_head
{
this:
np:hasAssertion
dgn-np:NP44185.RA4rmJPwPgvDfv8nixoQtkZ8xQjIoJpFS9NQ_s4hV2SG0130_assertion
;
np:hasProvenance
dgn-np:NP44185.RA4rmJPwPgvDfv8nixoQtkZ8xQjIoJpFS9NQ_s4hV2SG0130_provenance
;
np:hasPublicationInfo
dgn-np:NP44185.RA4rmJPwPgvDfv8nixoQtkZ8xQjIoJpFS9NQ_s4hV2SG0130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP44185.RA4rmJPwPgvDfv8nixoQtkZ8xQjIoJpFS9NQ_s4hV2SG0130_assertion
a
np:Assertion
.
dgn-np:NP44185.RA4rmJPwPgvDfv8nixoQtkZ8xQjIoJpFS9NQ_s4hV2SG0130_provenance
a
np:Provenance
.
dgn-np:NP44185.RA4rmJPwPgvDfv8nixoQtkZ8xQjIoJpFS9NQ_s4hV2SG0130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP44185.RA4rmJPwPgvDfv8nixoQtkZ8xQjIoJpFS9NQ_s4hV2SG0130_assertion
{
miriam-gene:2200
a
ncit:C16612
.
lld:C0036421
a
ncit:C7057
.
dgn-gda:DGN4fb6c4daa829246f818022c7360011c4
sio:SIO_000628
miriam-gene:2200
,
lld:C0036421
;
a
sio:SIO_001122
.
}
dgn-np:NP44185.RA4rmJPwPgvDfv8nixoQtkZ8xQjIoJpFS9NQ_s4hV2SG0130_provenance
{
dgn-np:NP44185.RA4rmJPwPgvDfv8nixoQtkZ8xQjIoJpFS9NQ_s4hV2SG0130_assertion
dcterms:description
"[ A 2-cM haplotype on chromosome 15q that contains FBN1 is associated with scleroderma in Choctaw Native Americans from Oklahoma. This haplotype may have been inherited from common founders about 10 generations ago and may contribute to the high prevalence of SSc that is now seen.]. 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:9778214
;
prov:wasDerivedFrom
dgn-void:gad-20130706
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:gad-20130706
pav:importedOn
"2013-07-06"^^
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:NP44185.RA4rmJPwPgvDfv8nixoQtkZ8xQjIoJpFS9NQ_s4hV2SG0130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:32:20+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" .
}