Matches in Nanopublications for { <http://rdf.disgenet.org/nanopublications.trig#NP563415.RAW5eYSM7uvtj7VZt6wmqMmrFCHiH3h2Wl5eeu6t00STU130_assertion> ?p ?o ?g. }
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- NP563415.RAW5eYSM7uvtj7VZt6wmqMmrFCHiH3h2Wl5eeu6t00STU130_assertion type Assertion NP563415.RAW5eYSM7uvtj7VZt6wmqMmrFCHiH3h2Wl5eeu6t00STU130_head.
- NP563415.RAW5eYSM7uvtj7VZt6wmqMmrFCHiH3h2Wl5eeu6t00STU130_assertion description "[Mutations in LOXHD1, a recessive-deafness locus, cause dominant late-onset Fuchs corneal dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP563415.RAW5eYSM7uvtj7VZt6wmqMmrFCHiH3h2Wl5eeu6t00STU130_provenance.
- NP563415.RAW5eYSM7uvtj7VZt6wmqMmrFCHiH3h2Wl5eeu6t00STU130_assertion evidence source_evidence_literature NP563415.RAW5eYSM7uvtj7VZt6wmqMmrFCHiH3h2Wl5eeu6t00STU130_provenance.
- NP563415.RAW5eYSM7uvtj7VZt6wmqMmrFCHiH3h2Wl5eeu6t00STU130_assertion SIO_000772 22341973 NP563415.RAW5eYSM7uvtj7VZt6wmqMmrFCHiH3h2Wl5eeu6t00STU130_provenance.
- NP563415.RAW5eYSM7uvtj7VZt6wmqMmrFCHiH3h2Wl5eeu6t00STU130_assertion wasDerivedFrom befree-20140225 NP563415.RAW5eYSM7uvtj7VZt6wmqMmrFCHiH3h2Wl5eeu6t00STU130_provenance.
- NP563415.RAW5eYSM7uvtj7VZt6wmqMmrFCHiH3h2Wl5eeu6t00STU130_assertion wasGeneratedBy ECO_0000203 NP563415.RAW5eYSM7uvtj7VZt6wmqMmrFCHiH3h2Wl5eeu6t00STU130_provenance.