Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP927921.RAwvJFRgsygtpzOJfGINijFo2a7dMiFzXZoGxA8xKDPdQ130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP927921.RAwvJFRgsygtpzOJfGINijFo2a7dMiFzXZoGxA8xKDPdQ130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP927921.RAwvJFRgsygtpzOJfGINijFo2a7dMiFzXZoGxA8xKDPdQ130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP927921.RAwvJFRgsygtpzOJfGINijFo2a7dMiFzXZoGxA8xKDPdQ130_provenance.
- NP927921.RAwvJFRgsygtpzOJfGINijFo2a7dMiFzXZoGxA8xKDPdQ130_assertion description "[Mutations in the human ATGL gene are associated with neutral lipid storage disease with myopathy, a rare genetic disease characterized by excessive accumulation of TG in multiple tissues.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP927921.RAwvJFRgsygtpzOJfGINijFo2a7dMiFzXZoGxA8xKDPdQ130_provenance.
- NP927921.RAwvJFRgsygtpzOJfGINijFo2a7dMiFzXZoGxA8xKDPdQ130_assertion evidence source_evidence_literature NP927921.RAwvJFRgsygtpzOJfGINijFo2a7dMiFzXZoGxA8xKDPdQ130_provenance.
- NP927921.RAwvJFRgsygtpzOJfGINijFo2a7dMiFzXZoGxA8xKDPdQ130_assertion SIO_000772 21828047 NP927921.RAwvJFRgsygtpzOJfGINijFo2a7dMiFzXZoGxA8xKDPdQ130_provenance.
- NP927921.RAwvJFRgsygtpzOJfGINijFo2a7dMiFzXZoGxA8xKDPdQ130_assertion wasDerivedFrom befree-20150227 NP927921.RAwvJFRgsygtpzOJfGINijFo2a7dMiFzXZoGxA8xKDPdQ130_provenance.
- NP927921.RAwvJFRgsygtpzOJfGINijFo2a7dMiFzXZoGxA8xKDPdQ130_assertion wasGeneratedBy ECO_0000203 NP927921.RAwvJFRgsygtpzOJfGINijFo2a7dMiFzXZoGxA8xKDPdQ130_provenance.
- befree-20150227 importedOn "2015-02-27" NP927921.RAwvJFRgsygtpzOJfGINijFo2a7dMiFzXZoGxA8xKDPdQ130_provenance.