@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP335869.RAkv943SGM2TcGMGj2gVr9VFAUvSAKgBjSD5lIIxC9sgE
> .
@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:NP335869.RAkv943SGM2TcGMGj2gVr9VFAUvSAKgBjSD5lIIxC9sgE130_head
{
this:
np:hasAssertion
dgn-np:NP335869.RAkv943SGM2TcGMGj2gVr9VFAUvSAKgBjSD5lIIxC9sgE130_assertion
;
np:hasProvenance
dgn-np:NP335869.RAkv943SGM2TcGMGj2gVr9VFAUvSAKgBjSD5lIIxC9sgE130_provenance
;
np:hasPublicationInfo
dgn-np:NP335869.RAkv943SGM2TcGMGj2gVr9VFAUvSAKgBjSD5lIIxC9sgE130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP335869.RAkv943SGM2TcGMGj2gVr9VFAUvSAKgBjSD5lIIxC9sgE130_assertion
a
np:Assertion
.
dgn-np:NP335869.RAkv943SGM2TcGMGj2gVr9VFAUvSAKgBjSD5lIIxC9sgE130_provenance
a
np:Provenance
.
dgn-np:NP335869.RAkv943SGM2TcGMGj2gVr9VFAUvSAKgBjSD5lIIxC9sgE130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP335869.RAkv943SGM2TcGMGj2gVr9VFAUvSAKgBjSD5lIIxC9sgE130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0024523
a
ncit:C7057
.
dgn-gda:DGN2a2ef70e456f1a2b1d53a40910b17921
sio:SIO_000628
miriam-gene:1080
,
lld:C0024523
;
a
sio:SIO_001121
.
}
dgn-np:NP335869.RAkv943SGM2TcGMGj2gVr9VFAUvSAKgBjSD5lIIxC9sgE130_provenance
{
dgn-np:NP335869.RAkv943SGM2TcGMGj2gVr9VFAUvSAKgBjSD5lIIxC9sgE130_assertion
dcterms:description
"[Collectively, these results highlight the role played by CFTR in intestinal handling of lipids and may suggest that factors other than defective CFTR are responsible for the abnormal intracellular events leading to fat malabsorption in CF patients.]. 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:19808659
;
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:NP335869.RAkv943SGM2TcGMGj2gVr9VFAUvSAKgBjSD5lIIxC9sgE130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:17+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" .
}