Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP648936.RAg357-0s9SDWVgp62KrKNT5i7gLxZIviBIclxDtYspCI130_assertion> ?p ?o ?g. }
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- NP648936.RAg357-0s9SDWVgp62KrKNT5i7gLxZIviBIclxDtYspCI130_assertion type Assertion NP648936.RAg357-0s9SDWVgp62KrKNT5i7gLxZIviBIclxDtYspCI130_head.
- NP648936.RAg357-0s9SDWVgp62KrKNT5i7gLxZIviBIclxDtYspCI130_assertion wasGeneratedBy ECO_0000203 NP648936.RAg357-0s9SDWVgp62KrKNT5i7gLxZIviBIclxDtYspCI130_provenance.
- NP648936.RAg357-0s9SDWVgp62KrKNT5i7gLxZIviBIclxDtYspCI130_assertion wasDerivedFrom befree-20140225 NP648936.RAg357-0s9SDWVgp62KrKNT5i7gLxZIviBIclxDtYspCI130_provenance.
- NP648936.RAg357-0s9SDWVgp62KrKNT5i7gLxZIviBIclxDtYspCI130_assertion SIO_000772 23176487 NP648936.RAg357-0s9SDWVgp62KrKNT5i7gLxZIviBIclxDtYspCI130_provenance.
- NP648936.RAg357-0s9SDWVgp62KrKNT5i7gLxZIviBIclxDtYspCI130_assertion evidence source_evidence_literature NP648936.RAg357-0s9SDWVgp62KrKNT5i7gLxZIviBIclxDtYspCI130_provenance.
- NP648936.RAg357-0s9SDWVgp62KrKNT5i7gLxZIviBIclxDtYspCI130_assertion description "[Martsolf syndrome has been associated with a mutation in RAB3GAP2.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP648936.RAg357-0s9SDWVgp62KrKNT5i7gLxZIviBIclxDtYspCI130_provenance.