Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1017431.RAv0E6apJ8F1FpCTcJzaDm00r4795QCrn1HTySaxBtylM130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1017431.RAv0E6apJ8F1FpCTcJzaDm00r4795QCrn1HTySaxBtylM130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1017431.RAv0E6apJ8F1FpCTcJzaDm00r4795QCrn1HTySaxBtylM130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1017431.RAv0E6apJ8F1FpCTcJzaDm00r4795QCrn1HTySaxBtylM130_provenance.
- NP1017431.RAv0E6apJ8F1FpCTcJzaDm00r4795QCrn1HTySaxBtylM130_assertion description "[The patient harboring the c.249-1G>A mutation exhibited isolated growth hormone deficiency at diagnosis and a gradual loss of ACTH, whereas the patient with the p.V75I mutation exhibited multiple pituitary hormone deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1017431.RAv0E6apJ8F1FpCTcJzaDm00r4795QCrn1HTySaxBtylM130_provenance.
- NP1017431.RAv0E6apJ8F1FpCTcJzaDm00r4795QCrn1HTySaxBtylM130_assertion evidence source_evidence_literature NP1017431.RAv0E6apJ8F1FpCTcJzaDm00r4795QCrn1HTySaxBtylM130_provenance.
- NP1017431.RAv0E6apJ8F1FpCTcJzaDm00r4795QCrn1HTySaxBtylM130_assertion SIO_000772 23029363 NP1017431.RAv0E6apJ8F1FpCTcJzaDm00r4795QCrn1HTySaxBtylM130_provenance.
- NP1017431.RAv0E6apJ8F1FpCTcJzaDm00r4795QCrn1HTySaxBtylM130_assertion wasDerivedFrom befree-2016 NP1017431.RAv0E6apJ8F1FpCTcJzaDm00r4795QCrn1HTySaxBtylM130_provenance.
- NP1017431.RAv0E6apJ8F1FpCTcJzaDm00r4795QCrn1HTySaxBtylM130_assertion wasGeneratedBy ECO_0000203 NP1017431.RAv0E6apJ8F1FpCTcJzaDm00r4795QCrn1HTySaxBtylM130_provenance.
- befree-2016 importedOn "2016-02-19" NP1017431.RAv0E6apJ8F1FpCTcJzaDm00r4795QCrn1HTySaxBtylM130_provenance.