Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP532769.RAYXMd-62xMK3B0Y4-QAfk8tbVZNLC9a-PNhg6WQLJ2JM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP532769.RAYXMd-62xMK3B0Y4-QAfk8tbVZNLC9a-PNhg6WQLJ2JM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP532769.RAYXMd-62xMK3B0Y4-QAfk8tbVZNLC9a-PNhg6WQLJ2JM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP532769.RAYXMd-62xMK3B0Y4-QAfk8tbVZNLC9a-PNhg6WQLJ2JM130_provenance.
- NP532769.RAYXMd-62xMK3B0Y4-QAfk8tbVZNLC9a-PNhg6WQLJ2JM130_assertion description "[A novel germline mutation of the PTEN gene in a patient with macrocephaly, ventricular dilatation, and features of VATER association.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP532769.RAYXMd-62xMK3B0Y4-QAfk8tbVZNLC9a-PNhg6WQLJ2JM130_provenance.
- NP532769.RAYXMd-62xMK3B0Y4-QAfk8tbVZNLC9a-PNhg6WQLJ2JM130_assertion evidence source_evidence_literature NP532769.RAYXMd-62xMK3B0Y4-QAfk8tbVZNLC9a-PNhg6WQLJ2JM130_provenance.
- NP532769.RAYXMd-62xMK3B0Y4-QAfk8tbVZNLC9a-PNhg6WQLJ2JM130_assertion SIO_000772 11748304 NP532769.RAYXMd-62xMK3B0Y4-QAfk8tbVZNLC9a-PNhg6WQLJ2JM130_provenance.
- NP532769.RAYXMd-62xMK3B0Y4-QAfk8tbVZNLC9a-PNhg6WQLJ2JM130_assertion wasDerivedFrom befree-20140225 NP532769.RAYXMd-62xMK3B0Y4-QAfk8tbVZNLC9a-PNhg6WQLJ2JM130_provenance.
- NP532769.RAYXMd-62xMK3B0Y4-QAfk8tbVZNLC9a-PNhg6WQLJ2JM130_assertion wasGeneratedBy ECO_0000203 NP532769.RAYXMd-62xMK3B0Y4-QAfk8tbVZNLC9a-PNhg6WQLJ2JM130_provenance.
- befree-20140225 importedOn "2014-02-25" NP532769.RAYXMd-62xMK3B0Y4-QAfk8tbVZNLC9a-PNhg6WQLJ2JM130_provenance.