Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP553658.RA2KILyElaRJLIzL6UCvBJpl6W3ygPZFDJglre6AGhlfw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP553658.RA2KILyElaRJLIzL6UCvBJpl6W3ygPZFDJglre6AGhlfw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP553658.RA2KILyElaRJLIzL6UCvBJpl6W3ygPZFDJglre6AGhlfw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP553658.RA2KILyElaRJLIzL6UCvBJpl6W3ygPZFDJglre6AGhlfw130_provenance.
- NP553658.RA2KILyElaRJLIzL6UCvBJpl6W3ygPZFDJglre6AGhlfw130_assertion description "[Heterozygous germline mutations of the tumor-suppressor gene MEN1 are responsible for multiple endocrine neoplasia type 1 (MEN1), a dominantly inherited familial cancer syndrome characterized by pituitary, parathyroid, and enteropancreatic tumors.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP553658.RA2KILyElaRJLIzL6UCvBJpl6W3ygPZFDJglre6AGhlfw130_provenance.
- NP553658.RA2KILyElaRJLIzL6UCvBJpl6W3ygPZFDJglre6AGhlfw130_assertion evidence source_evidence_literature NP553658.RA2KILyElaRJLIzL6UCvBJpl6W3ygPZFDJglre6AGhlfw130_provenance.
- NP553658.RA2KILyElaRJLIzL6UCvBJpl6W3ygPZFDJglre6AGhlfw130_assertion SIO_000772 19068082 NP553658.RA2KILyElaRJLIzL6UCvBJpl6W3ygPZFDJglre6AGhlfw130_provenance.
- NP553658.RA2KILyElaRJLIzL6UCvBJpl6W3ygPZFDJglre6AGhlfw130_assertion wasDerivedFrom befree-20150227 NP553658.RA2KILyElaRJLIzL6UCvBJpl6W3ygPZFDJglre6AGhlfw130_provenance.
- NP553658.RA2KILyElaRJLIzL6UCvBJpl6W3ygPZFDJglre6AGhlfw130_assertion wasGeneratedBy ECO_0000203 NP553658.RA2KILyElaRJLIzL6UCvBJpl6W3ygPZFDJglre6AGhlfw130_provenance.
- befree-20150227 importedOn "2015-02-27" NP553658.RA2KILyElaRJLIzL6UCvBJpl6W3ygPZFDJglre6AGhlfw130_provenance.