Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP562396.RAcKzNqF1F2JQ2yfHW7wP7HtROF2VpRN-gEJ6u60D9d9A130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP562396.RAcKzNqF1F2JQ2yfHW7wP7HtROF2VpRN-gEJ6u60D9d9A130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP562396.RAcKzNqF1F2JQ2yfHW7wP7HtROF2VpRN-gEJ6u60D9d9A130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP562396.RAcKzNqF1F2JQ2yfHW7wP7HtROF2VpRN-gEJ6u60D9d9A130_provenance.
- NP562396.RAcKzNqF1F2JQ2yfHW7wP7HtROF2VpRN-gEJ6u60D9d9A130_assertion description "[PROP1 gene mutations lead to combined pituitary deficiency, and HESX gene mutations result in septo-optic dysplasia, both of which include HH.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP562396.RAcKzNqF1F2JQ2yfHW7wP7HtROF2VpRN-gEJ6u60D9d9A130_provenance.
- NP562396.RAcKzNqF1F2JQ2yfHW7wP7HtROF2VpRN-gEJ6u60D9d9A130_assertion evidence source_evidence_literature NP562396.RAcKzNqF1F2JQ2yfHW7wP7HtROF2VpRN-gEJ6u60D9d9A130_provenance.
- NP562396.RAcKzNqF1F2JQ2yfHW7wP7HtROF2VpRN-gEJ6u60D9d9A130_assertion SIO_000772 10727999 NP562396.RAcKzNqF1F2JQ2yfHW7wP7HtROF2VpRN-gEJ6u60D9d9A130_provenance.
- NP562396.RAcKzNqF1F2JQ2yfHW7wP7HtROF2VpRN-gEJ6u60D9d9A130_assertion wasDerivedFrom befree-20140225 NP562396.RAcKzNqF1F2JQ2yfHW7wP7HtROF2VpRN-gEJ6u60D9d9A130_provenance.
- NP562396.RAcKzNqF1F2JQ2yfHW7wP7HtROF2VpRN-gEJ6u60D9d9A130_assertion wasGeneratedBy ECO_0000203 NP562396.RAcKzNqF1F2JQ2yfHW7wP7HtROF2VpRN-gEJ6u60D9d9A130_provenance.
- befree-20140225 importedOn "2014-02-25" NP562396.RAcKzNqF1F2JQ2yfHW7wP7HtROF2VpRN-gEJ6u60D9d9A130_provenance.