@prefix this: <
http://rdf.disgenet.org/resource/nanopub/NP1005559.RAZ7Lclum4t9uIzfzDMDPbgJtuzpZdJXRulL8jO8M6Fgo
> .
@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/v3.0.0/void/
> .
dgn-np:NP1005559.RAZ7Lclum4t9uIzfzDMDPbgJtuzpZdJXRulL8jO8M6Fgo130_head
{
this:
np:hasAssertion
dgn-np:NP1005559.RAZ7Lclum4t9uIzfzDMDPbgJtuzpZdJXRulL8jO8M6Fgo130_assertion
;
np:hasProvenance
dgn-np:NP1005559.RAZ7Lclum4t9uIzfzDMDPbgJtuzpZdJXRulL8jO8M6Fgo130_provenance
;
np:hasPublicationInfo
dgn-np:NP1005559.RAZ7Lclum4t9uIzfzDMDPbgJtuzpZdJXRulL8jO8M6Fgo130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP1005559.RAZ7Lclum4t9uIzfzDMDPbgJtuzpZdJXRulL8jO8M6Fgo130_assertion
a
np:Assertion
.
dgn-np:NP1005559.RAZ7Lclum4t9uIzfzDMDPbgJtuzpZdJXRulL8jO8M6Fgo130_provenance
a
np:Provenance
.
dgn-np:NP1005559.RAZ7Lclum4t9uIzfzDMDPbgJtuzpZdJXRulL8jO8M6Fgo130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP1005559.RAZ7Lclum4t9uIzfzDMDPbgJtuzpZdJXRulL8jO8M6Fgo130_assertion
{
miriam-gene:653509
a
ncit:C16612
.
lld:C0694549
a
ncit:C7057
.
dgn-gda:DGNab7ccdedbc283a1eb72f9f698baf0fac
sio:SIO_000628
miriam-gene:653509
,
lld:C0694549
;
a
sio:SIO_001121
.
}
dgn-np:NP1005559.RAZ7Lclum4t9uIzfzDMDPbgJtuzpZdJXRulL8jO8M6Fgo130_provenance
{
dgn-np:NP1005559.RAZ7Lclum4t9uIzfzDMDPbgJtuzpZdJXRulL8jO8M6Fgo130_assertion
dcterms:description
"[Our study indicates that missense single nucleotide polymorphisms and haplotypes of SFTPA1, SFTPA2 and SFTPD are associated with susceptibility to CAP, and that several haplotypes also influence severity and outcome of CAP.]. 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:21310059
;
prov:wasDerivedFrom
dgn-void:befree-20150227
;
prov:wasGeneratedBy
eco:ECO_0000203
.
dgn-void:befree-20150227
pav:importedOn
"2015-02-27"^^
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:NP1005559.RAZ7Lclum4t9uIzfzDMDPbgJtuzpZdJXRulL8jO8M6Fgo130_publicationInfo
{
this:
dcterms:created
"2015-08-25T14:48:03+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
"v3.0.0.0" .
dgn-void:disgenetv3.0rdf
pav:version
"v3.0.0" .
}