Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP7569.RA4J2wSj1r0VZZaLeCv1ehyEYyFSng6OaOWnvoe77zsco130_assertion> ?p ?o ?g. }
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- NP7569.RA4J2wSj1r0VZZaLeCv1ehyEYyFSng6OaOWnvoe77zsco130_assertion type Assertion NP7569.RA4J2wSj1r0VZZaLeCv1ehyEYyFSng6OaOWnvoe77zsco130_head.
- NP7569.RA4J2wSj1r0VZZaLeCv1ehyEYyFSng6OaOWnvoe77zsco130_assertion description "[The syndrome of microcornea, myopic chorioretinal atrophy, and telecanthus (MMCAT) is caused by mutations in ADAMTS18.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP7569.RA4J2wSj1r0VZZaLeCv1ehyEYyFSng6OaOWnvoe77zsco130_provenance.
- NP7569.RA4J2wSj1r0VZZaLeCv1ehyEYyFSng6OaOWnvoe77zsco130_assertion evidence source_evidence_curated NP7569.RA4J2wSj1r0VZZaLeCv1ehyEYyFSng6OaOWnvoe77zsco130_provenance.
- NP7569.RA4J2wSj1r0VZZaLeCv1ehyEYyFSng6OaOWnvoe77zsco130_assertion SIO_000772 23818446 NP7569.RA4J2wSj1r0VZZaLeCv1ehyEYyFSng6OaOWnvoe77zsco130_provenance.
- NP7569.RA4J2wSj1r0VZZaLeCv1ehyEYyFSng6OaOWnvoe77zsco130_assertion wasDerivedFrom uniprot-2016 NP7569.RA4J2wSj1r0VZZaLeCv1ehyEYyFSng6OaOWnvoe77zsco130_provenance.
- NP7569.RA4J2wSj1r0VZZaLeCv1ehyEYyFSng6OaOWnvoe77zsco130_assertion wasGeneratedBy ECO_0000218 NP7569.RA4J2wSj1r0VZZaLeCv1ehyEYyFSng6OaOWnvoe77zsco130_provenance.