Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP762989.RAVi5tcsaKVyYbcd1mFRrAwDsEvV0FM9l6B_WkQoeIRmM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP762989.RAVi5tcsaKVyYbcd1mFRrAwDsEvV0FM9l6B_WkQoeIRmM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP762989.RAVi5tcsaKVyYbcd1mFRrAwDsEvV0FM9l6B_WkQoeIRmM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP762989.RAVi5tcsaKVyYbcd1mFRrAwDsEvV0FM9l6B_WkQoeIRmM130_provenance.
- NP762989.RAVi5tcsaKVyYbcd1mFRrAwDsEvV0FM9l6B_WkQoeIRmM130_assertion description "[We report here the molecular genetic detection of an alteration of the A2M gene in a patient with serum A2M deficiency and chronic lung disease since childhood.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP762989.RAVi5tcsaKVyYbcd1mFRrAwDsEvV0FM9l6B_WkQoeIRmM130_provenance.
- NP762989.RAVi5tcsaKVyYbcd1mFRrAwDsEvV0FM9l6B_WkQoeIRmM130_assertion evidence source_evidence_literature NP762989.RAVi5tcsaKVyYbcd1mFRrAwDsEvV0FM9l6B_WkQoeIRmM130_provenance.
- NP762989.RAVi5tcsaKVyYbcd1mFRrAwDsEvV0FM9l6B_WkQoeIRmM130_assertion SIO_000772 2475424 NP762989.RAVi5tcsaKVyYbcd1mFRrAwDsEvV0FM9l6B_WkQoeIRmM130_provenance.
- NP762989.RAVi5tcsaKVyYbcd1mFRrAwDsEvV0FM9l6B_WkQoeIRmM130_assertion wasDerivedFrom befree-20140225 NP762989.RAVi5tcsaKVyYbcd1mFRrAwDsEvV0FM9l6B_WkQoeIRmM130_provenance.
- NP762989.RAVi5tcsaKVyYbcd1mFRrAwDsEvV0FM9l6B_WkQoeIRmM130_assertion wasGeneratedBy ECO_0000203 NP762989.RAVi5tcsaKVyYbcd1mFRrAwDsEvV0FM9l6B_WkQoeIRmM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP762989.RAVi5tcsaKVyYbcd1mFRrAwDsEvV0FM9l6B_WkQoeIRmM130_provenance.