@prefix this: <
http://rdf.disgenet.org/nanopublications.trig#NP694830.RAI_ID8QizzaJVrppHbyiBvmjHonKJFwDqpIC0icokr5g
> .
@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:NP694830.RAI_ID8QizzaJVrppHbyiBvmjHonKJFwDqpIC0icokr5g130_head
{
this:
np:hasAssertion
dgn-np:NP694830.RAI_ID8QizzaJVrppHbyiBvmjHonKJFwDqpIC0icokr5g130_assertion
;
np:hasProvenance
dgn-np:NP694830.RAI_ID8QizzaJVrppHbyiBvmjHonKJFwDqpIC0icokr5g130_provenance
;
np:hasPublicationInfo
dgn-np:NP694830.RAI_ID8QizzaJVrppHbyiBvmjHonKJFwDqpIC0icokr5g130_publicationInfo
;
a
np:Nanopublication
.
dgn-np:NP694830.RAI_ID8QizzaJVrppHbyiBvmjHonKJFwDqpIC0icokr5g130_assertion
a
np:Assertion
.
dgn-np:NP694830.RAI_ID8QizzaJVrppHbyiBvmjHonKJFwDqpIC0icokr5g130_provenance
a
np:Provenance
.
dgn-np:NP694830.RAI_ID8QizzaJVrppHbyiBvmjHonKJFwDqpIC0icokr5g130_publicationInfo
a
np:PublicationInfo
.
}
dgn-np:NP694830.RAI_ID8QizzaJVrppHbyiBvmjHonKJFwDqpIC0icokr5g130_assertion
{
miriam-gene:7249
a
ncit:C16612
.
lld:C0007097
a
ncit:C7057
.
dgn-gda:DGNd6509fad6bbee90d5cb17865b114486b
sio:SIO_000628
miriam-gene:7249
,
lld:C0007097
;
a
sio:SIO_001121
.
}
dgn-np:NP694830.RAI_ID8QizzaJVrppHbyiBvmjHonKJFwDqpIC0icokr5g130_provenance
{
dgn-np:NP694830.RAI_ID8QizzaJVrppHbyiBvmjHonKJFwDqpIC0icokr5g130_assertion
dcterms:description
"[The identified truncation is the first genetic defect described for the laminin alpha1 chain and suggests that mutations in the LAM A1 gene might underlie the observed lack of the laminin alpha1 chain in some colon carcinomas.]. 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:10222155
;
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:NP694830.RAI_ID8QizzaJVrppHbyiBvmjHonKJFwDqpIC0icokr5g130_publicationInfo
{
this:
dcterms:created
"2014-10-02T12:39:02+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" .
}