@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1401091.RAIUPxB2MsEZ0P13s1cWA522_VrYcd56ccMv8Uj3BTu6c
> .
@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:NP1401091.RAIUPxB2MsEZ0P13s1cWA522_VrYcd56ccMv8Uj3BTu6c130_head
{
this:
np:hasAssertion
dgn-np:NP1401091.RAIUPxB2MsEZ0P13s1cWA522_VrYcd56ccMv8Uj3BTu6c130_assertion
;
np:hasProvenance
dgn-np:NP1401091.RAIUPxB2MsEZ0P13s1cWA522_VrYcd56ccMv8Uj3BTu6c130_provenance
;
np:hasPublicationInfo
dgn-np:NP1401091.RAIUPxB2MsEZ0P13s1cWA522_VrYcd56ccMv8Uj3BTu6c130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1401091.RAIUPxB2MsEZ0P13s1cWA522_VrYcd56ccMv8Uj3BTu6c130_assertion
a
np:Assertion
.
dgn-np:NP1401091.RAIUPxB2MsEZ0P13s1cWA522_VrYcd56ccMv8Uj3BTu6c130_provenance
a
np:Provenance
.
dgn-np:NP1401091.RAIUPxB2MsEZ0P13s1cWA522_VrYcd56ccMv8Uj3BTu6c130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1401091.RAIUPxB2MsEZ0P13s1cWA522_VrYcd56ccMv8Uj3BTu6c130_assertion
{
miriam-gene:1080
a
ncit:C16612
.
lld:C0010674
a
ncit:C7057
.
dgn-gda:DGN2d27b9708c8c00e7af7e36273ef7fa46
sio:SIO_000628
miriam-gene:1080
,
lld:C0010674
;
a
sio:SIO_001121
.
}
dgn-np:NP1401091.RAIUPxB2MsEZ0P13s1cWA522_VrYcd56ccMv8Uj3BTu6c130_provenance
{
dgn-np:NP1401091.RAIUPxB2MsEZ0P13s1cWA522_VrYcd56ccMv8Uj3BTu6c130_assertion
dcterms:description
"[Absence, dysfunction or low levels of cystic fibrosis (CF) transmembrane conductance regulator (CFTR) protein result in a broad range of clinical manifestations with CF with pancreatic insufficiency at the severe end of the phenotypic spectrum and, at the other end relatively mild clinical conditions, including several forms of male infertility.]. 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:9692018
;
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:NP1401091.RAIUPxB2MsEZ0P13s1cWA522_VrYcd56ccMv8Uj3BTu6c130_publicationInfo
{
this:
dcterms:created
"2016-05-13T12:52:21+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" .
}