Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP570038.RAAvdkrEZXHQLm3AYVN1aTCrxrJaevULxI4g2KuXPMV_g130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP570038.RAAvdkrEZXHQLm3AYVN1aTCrxrJaevULxI4g2KuXPMV_g130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP570038.RAAvdkrEZXHQLm3AYVN1aTCrxrJaevULxI4g2KuXPMV_g130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP570038.RAAvdkrEZXHQLm3AYVN1aTCrxrJaevULxI4g2KuXPMV_g130_provenance.
- NP570038.RAAvdkrEZXHQLm3AYVN1aTCrxrJaevULxI4g2KuXPMV_g130_assertion description "[Phenotypic variability was observed among patients with the same mutations, particularly the presence and age of onset of hypocortisolism, the levels of PRL and the results of pituitary imaging.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP570038.RAAvdkrEZXHQLm3AYVN1aTCrxrJaevULxI4g2KuXPMV_g130_provenance.
- NP570038.RAAvdkrEZXHQLm3AYVN1aTCrxrJaevULxI4g2KuXPMV_g130_assertion evidence source_evidence_literature NP570038.RAAvdkrEZXHQLm3AYVN1aTCrxrJaevULxI4g2KuXPMV_g130_provenance.
- NP570038.RAAvdkrEZXHQLm3AYVN1aTCrxrJaevULxI4g2KuXPMV_g130_assertion SIO_000772 16984240 NP570038.RAAvdkrEZXHQLm3AYVN1aTCrxrJaevULxI4g2KuXPMV_g130_provenance.
- NP570038.RAAvdkrEZXHQLm3AYVN1aTCrxrJaevULxI4g2KuXPMV_g130_assertion wasDerivedFrom befree-2016 NP570038.RAAvdkrEZXHQLm3AYVN1aTCrxrJaevULxI4g2KuXPMV_g130_provenance.
- NP570038.RAAvdkrEZXHQLm3AYVN1aTCrxrJaevULxI4g2KuXPMV_g130_assertion wasGeneratedBy ECO_0000203 NP570038.RAAvdkrEZXHQLm3AYVN1aTCrxrJaevULxI4g2KuXPMV_g130_provenance.
- befree-2016 importedOn "2016-02-19" NP570038.RAAvdkrEZXHQLm3AYVN1aTCrxrJaevULxI4g2KuXPMV_g130_provenance.