Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP208219.RAypAV4zbj--gkwk2Pz2kQdiBkCZlqQe_ABWLZIQ0OPMU130_assertion> ?p ?o ?g. }
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- NP208219.RAypAV4zbj--gkwk2Pz2kQdiBkCZlqQe_ABWLZIQ0OPMU130_assertion type Assertion NP208219.RAypAV4zbj--gkwk2Pz2kQdiBkCZlqQe_ABWLZIQ0OPMU130_head.
- NP208219.RAypAV4zbj--gkwk2Pz2kQdiBkCZlqQe_ABWLZIQ0OPMU130_assertion wasGeneratedBy ECO_0000203 NP208219.RAypAV4zbj--gkwk2Pz2kQdiBkCZlqQe_ABWLZIQ0OPMU130_provenance.
- NP208219.RAypAV4zbj--gkwk2Pz2kQdiBkCZlqQe_ABWLZIQ0OPMU130_assertion wasDerivedFrom lhgdn-20090331 NP208219.RAypAV4zbj--gkwk2Pz2kQdiBkCZlqQe_ABWLZIQ0OPMU130_provenance.
- NP208219.RAypAV4zbj--gkwk2Pz2kQdiBkCZlqQe_ABWLZIQ0OPMU130_assertion SIO_000772 15563506 NP208219.RAypAV4zbj--gkwk2Pz2kQdiBkCZlqQe_ABWLZIQ0OPMU130_provenance.
- NP208219.RAypAV4zbj--gkwk2Pz2kQdiBkCZlqQe_ABWLZIQ0OPMU130_assertion evidence source_evidence_literature NP208219.RAypAV4zbj--gkwk2Pz2kQdiBkCZlqQe_ABWLZIQ0OPMU130_provenance.
- NP208219.RAypAV4zbj--gkwk2Pz2kQdiBkCZlqQe_ABWLZIQ0OPMU130_assertion description "[dominant mutations are common in Ullrich congenital muscular dystrophy (UCMD).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP208219.RAypAV4zbj--gkwk2Pz2kQdiBkCZlqQe_ABWLZIQ0OPMU130_provenance.