@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc
> .
@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:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_head
{
this:
np:hasAssertion
dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_assertion
;
np:hasProvenance
dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_provenance
;
np:hasPublicationInfo
dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_assertion
a
np:Assertion
.
dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_provenance
a
np:Provenance
.
dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_assertion
{
miriam-gene:25981
a
ncit:C16612
.
lld:C0022521
a
ncit:C7057
.
dgn-gda:DGNe75739402458afa8bd4136401e6a0d94
sio:SIO_000628
miriam-gene:25981
,
lld:C0022521
;
a
sio:SIO_001121
.
}
dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_provenance
{
dgn-np:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_assertion
dcterms:description
"[The phenotype of MDHC7(-/-) mice is similar to that observed in some patients suffering from PCD, and our data strongly suggest that in some patients this disease could be due to mutations in the homologous human gene DNAH1 (HDHC7).]. 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:11371505
;
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:NP324428.RAV7nAUrHeFsnYy87MU6OohfYbKgG9WrxAYfMEDqVC2wc130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:35:09+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" .
}