Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_assertion> ?p ?o ?g. }
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- NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_assertion type Assertion NP185.RA3y-YkaxscQm5l_ohDZ0TZtF7vWDdYVjEgztDvQdJL6E130_head.
- 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.