Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_provenance.
- NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_assertion description "[Loss-of-function mutations in the human GLI2 gene are associated with pituitary anomalies and holoprosencephaly-like features.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_provenance.
- NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_assertion evidence source_evidence_literature NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_provenance.
- NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_assertion SIO_000772 14581620 NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_provenance.
- NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_assertion wasDerivedFrom befree-20150227 NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_provenance.
- NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_assertion wasGeneratedBy ECO_0000203 NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_provenance.
- befree-20150227 importedOn "2015-02-27" NP428418.RAE1YAsWN6aRd2OGGR2WjmDSodWZDz_C0aFm2FkvF8TNI130_provenance.