Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_provenance.
- NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_assertion description "[The high rate of detection of mutations by genomic sequencing of ALK-1 suggests that this will be a useful diagnostic test for HHT2, particularly where preliminary linkage to chromosome 12q13 can be established.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_provenance.
- NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_assertion evidence source_evidence_curated NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_provenance.
- NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_assertion SIO_000772 9245985 NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_provenance.
- NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_assertion wasDerivedFrom uniprot-20130724 NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_provenance.
- NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_assertion wasGeneratedBy ECO_0000218 NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_provenance.
- uniprot-20130724 importedOn "2013-07-24" NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_provenance.