@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP492242.RATZnDoWPiBq5Ehgo-zBhuRpv1BCyinGz02vtYcFkBsik
> .
@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:NP492242.RATZnDoWPiBq5Ehgo-zBhuRpv1BCyinGz02vtYcFkBsik130_head
{
this:
np:hasAssertion
dgn-np:NP492242.RATZnDoWPiBq5Ehgo-zBhuRpv1BCyinGz02vtYcFkBsik130_assertion
;
np:hasProvenance
dgn-np:NP492242.RATZnDoWPiBq5Ehgo-zBhuRpv1BCyinGz02vtYcFkBsik130_provenance
;
np:hasPublicationInfo
dgn-np:NP492242.RATZnDoWPiBq5Ehgo-zBhuRpv1BCyinGz02vtYcFkBsik130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP492242.RATZnDoWPiBq5Ehgo-zBhuRpv1BCyinGz02vtYcFkBsik130_assertion
a
np:Assertion
.
dgn-np:NP492242.RATZnDoWPiBq5Ehgo-zBhuRpv1BCyinGz02vtYcFkBsik130_provenance
a
np:Provenance
.
dgn-np:NP492242.RATZnDoWPiBq5Ehgo-zBhuRpv1BCyinGz02vtYcFkBsik130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP492242.RATZnDoWPiBq5Ehgo-zBhuRpv1BCyinGz02vtYcFkBsik130_assertion
{
miriam-gene:8195
a
ncit:C16612
.
lld:C0265215
a
ncit:C7057
.
dgn-gda:DGN79e20750bf7e737f920fe75e4b8da4d3
sio:SIO_000628
miriam-gene:8195
,
lld:C0265215
;
a
sio:SIO_001121
.
}
dgn-np:NP492242.RATZnDoWPiBq5Ehgo-zBhuRpv1BCyinGz02vtYcFkBsik130_provenance
{
dgn-np:NP492242.RATZnDoWPiBq5Ehgo-zBhuRpv1BCyinGz02vtYcFkBsik130_assertion
dcterms:description
"[Finally, we have analyzed genes present in the other Meckel syndrome critical regions, MKS2 and MKS3, to determine whether any of the candidate genes for the three MKS loci have similar gene functions or are members of a common biological pathway.]. 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:15112103
;
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:NP492242.RATZnDoWPiBq5Ehgo-zBhuRpv1BCyinGz02vtYcFkBsik130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:36:54+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" .
}