@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP239018.RArL4qS4J1djQz7hHbfTSIhcc9zXJnti_1YLZkwUEd69s
> .
@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:NP239018.RArL4qS4J1djQz7hHbfTSIhcc9zXJnti_1YLZkwUEd69s130_head
{
this:
np:hasAssertion
dgn-np:NP239018.RArL4qS4J1djQz7hHbfTSIhcc9zXJnti_1YLZkwUEd69s130_assertion
;
np:hasProvenance
dgn-np:NP239018.RArL4qS4J1djQz7hHbfTSIhcc9zXJnti_1YLZkwUEd69s130_provenance
;
np:hasPublicationInfo
dgn-np:NP239018.RArL4qS4J1djQz7hHbfTSIhcc9zXJnti_1YLZkwUEd69s130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP239018.RArL4qS4J1djQz7hHbfTSIhcc9zXJnti_1YLZkwUEd69s130_assertion
a
np:Assertion
.
dgn-np:NP239018.RArL4qS4J1djQz7hHbfTSIhcc9zXJnti_1YLZkwUEd69s130_provenance
a
np:Provenance
.
dgn-np:NP239018.RArL4qS4J1djQz7hHbfTSIhcc9zXJnti_1YLZkwUEd69s130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP239018.RArL4qS4J1djQz7hHbfTSIhcc9zXJnti_1YLZkwUEd69s130_assertion
{
miriam-gene:4153
a
ncit:C16612
.
lld:C1623038
a
ncit:C7057
.
dgn-gda:DGNbb118e189203623e127ff9f850a65380
sio:SIO_000628
miriam-gene:4153
,
lld:C1623038
;
a
sio:SIO_001121
.
}
dgn-np:NP239018.RArL4qS4J1djQz7hHbfTSIhcc9zXJnti_1YLZkwUEd69s130_provenance
{
dgn-np:NP239018.RArL4qS4J1djQz7hHbfTSIhcc9zXJnti_1YLZkwUEd69s130_assertion
dcterms:description
"[The modulating role of mannose binding lectin in the occurrence of cirrhosis in cystic fibrosis could be explained by the fact that hepatotoxic damage from viruses or bacteria might be increased by the immunodeficiency associated with mannose binding lectin variants and might facilitate the degradation of liver status.]. 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:11333866
;
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:NP239018.RArL4qS4J1djQz7hHbfTSIhcc9zXJnti_1YLZkwUEd69s130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:34:14+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" .
}