Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP1215292.RAH6NpIh71nfqR-Bqlui-ajizNX5aa_2Hci8EUokvYolw130_provenance>. }
Showing items 1 to 9 of
9
with 100 items per page.
- source_evidence_literature type ECO_0000212 NP1215292.RAH6NpIh71nfqR-Bqlui-ajizNX5aa_2Hci8EUokvYolw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP1215292.RAH6NpIh71nfqR-Bqlui-ajizNX5aa_2Hci8EUokvYolw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP1215292.RAH6NpIh71nfqR-Bqlui-ajizNX5aa_2Hci8EUokvYolw130_provenance.
- NP1215292.RAH6NpIh71nfqR-Bqlui-ajizNX5aa_2Hci8EUokvYolw130_assertion description "[Of 26 other reported recessive ECEL1 mutation cases (14 families), all had arthrogryposis, 19 had documented ptosis, and 4 had documented complex strabismus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1215292.RAH6NpIh71nfqR-Bqlui-ajizNX5aa_2Hci8EUokvYolw130_provenance.
- NP1215292.RAH6NpIh71nfqR-Bqlui-ajizNX5aa_2Hci8EUokvYolw130_assertion evidence source_evidence_literature NP1215292.RAH6NpIh71nfqR-Bqlui-ajizNX5aa_2Hci8EUokvYolw130_provenance.
- NP1215292.RAH6NpIh71nfqR-Bqlui-ajizNX5aa_2Hci8EUokvYolw130_assertion SIO_000772 25173900 NP1215292.RAH6NpIh71nfqR-Bqlui-ajizNX5aa_2Hci8EUokvYolw130_provenance.
- NP1215292.RAH6NpIh71nfqR-Bqlui-ajizNX5aa_2Hci8EUokvYolw130_assertion wasDerivedFrom befree-2016 NP1215292.RAH6NpIh71nfqR-Bqlui-ajizNX5aa_2Hci8EUokvYolw130_provenance.
- NP1215292.RAH6NpIh71nfqR-Bqlui-ajizNX5aa_2Hci8EUokvYolw130_assertion wasGeneratedBy ECO_0000203 NP1215292.RAH6NpIh71nfqR-Bqlui-ajizNX5aa_2Hci8EUokvYolw130_provenance.
- befree-2016 importedOn "2016-02-19" NP1215292.RAH6NpIh71nfqR-Bqlui-ajizNX5aa_2Hci8EUokvYolw130_provenance.