Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP991566.RAanCOV1qPyTHNWAjfS8K-PYa_Ezj1urX_QuRhcyenBfc130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP991566.RAanCOV1qPyTHNWAjfS8K-PYa_Ezj1urX_QuRhcyenBfc130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP991566.RAanCOV1qPyTHNWAjfS8K-PYa_Ezj1urX_QuRhcyenBfc130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP991566.RAanCOV1qPyTHNWAjfS8K-PYa_Ezj1urX_QuRhcyenBfc130_provenance.
- NP991566.RAanCOV1qPyTHNWAjfS8K-PYa_Ezj1urX_QuRhcyenBfc130_assertion description "[A novel OTX2 mutation in a patient with combined pituitary hormone deficiency, pituitary malformation, and an underdeveloped left optic nerve.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP991566.RAanCOV1qPyTHNWAjfS8K-PYa_Ezj1urX_QuRhcyenBfc130_provenance.
- NP991566.RAanCOV1qPyTHNWAjfS8K-PYa_Ezj1urX_QuRhcyenBfc130_assertion evidence source_evidence_literature NP991566.RAanCOV1qPyTHNWAjfS8K-PYa_Ezj1urX_QuRhcyenBfc130_provenance.
- NP991566.RAanCOV1qPyTHNWAjfS8K-PYa_Ezj1urX_QuRhcyenBfc130_assertion SIO_000772 22715480 NP991566.RAanCOV1qPyTHNWAjfS8K-PYa_Ezj1urX_QuRhcyenBfc130_provenance.
- NP991566.RAanCOV1qPyTHNWAjfS8K-PYa_Ezj1urX_QuRhcyenBfc130_assertion wasDerivedFrom befree-2016 NP991566.RAanCOV1qPyTHNWAjfS8K-PYa_Ezj1urX_QuRhcyenBfc130_provenance.
- NP991566.RAanCOV1qPyTHNWAjfS8K-PYa_Ezj1urX_QuRhcyenBfc130_assertion wasGeneratedBy ECO_0000203 NP991566.RAanCOV1qPyTHNWAjfS8K-PYa_Ezj1urX_QuRhcyenBfc130_provenance.
- befree-2016 importedOn "2016-02-19" NP991566.RAanCOV1qPyTHNWAjfS8K-PYa_Ezj1urX_QuRhcyenBfc130_provenance.