@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP417332.RAYxg3_6J1XTkA_LKeHtTdoil_FrbVy1WOdseD426DcyY
> .
@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#
> .
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{
this:
np:hasAssertion
dgn-np:NP417332.RAYxg3_6J1XTkA_LKeHtTdoil_FrbVy1WOdseD426DcyY130_assertion
;
np:hasProvenance
dgn-np:NP417332.RAYxg3_6J1XTkA_LKeHtTdoil_FrbVy1WOdseD426DcyY130_provenance
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np:hasPublicationInfo
dgn-np:NP417332.RAYxg3_6J1XTkA_LKeHtTdoil_FrbVy1WOdseD426DcyY130_publicationInfo
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a
np:Nanopublication
.
dgn-np:NP417332.RAYxg3_6J1XTkA_LKeHtTdoil_FrbVy1WOdseD426DcyY130_assertion
a
np:Assertion
.
dgn-np:NP417332.RAYxg3_6J1XTkA_LKeHtTdoil_FrbVy1WOdseD426DcyY130_provenance
a
np:Provenance
.
dgn-np:NP417332.RAYxg3_6J1XTkA_LKeHtTdoil_FrbVy1WOdseD426DcyY130_publicationInfo
a
np:PublicationInfo
.
}
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{
miriam-gene:727897
a
ncit:C16612
.
lld:C0206062
a
ncit:C7057
.
dgn-gda:DGN43deeef158d4bda514a7cab49106c622
sio:SIO_000628
miriam-gene:727897
,
lld:C0206062
;
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sio:SIO_001121
.
}
dgn-np:NP417332.RAYxg3_6J1XTkA_LKeHtTdoil_FrbVy1WOdseD426DcyY130_provenance
{
dgn-np:NP417332.RAYxg3_6J1XTkA_LKeHtTdoil_FrbVy1WOdseD426DcyY130_assertion
dcterms:description
"[This article reviews the genetic and environmental causes of pulmonary fibrosis, specifically focusing on genetic and epigenetic variants of MUC5B and several types of ILD, to discuss why only some individuals with the MUC5B promoter polymorphism develop pulmonary fibrosis.]. 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:22802285
;
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 .
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dgn-np:NP417332.RAYxg3_6J1XTkA_LKeHtTdoil_FrbVy1WOdseD426DcyY130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:08+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
<
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> , <
http://orcid.org/0000-0002-7534-7661
> , <
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> , <
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
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}