Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP583445.RANFAaIyenWo4fr1lMIqT4L-kS5qwXIpgq7Fsr6YMf9Jk130_assertion> ?p ?o ?g. }
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- NP583445.RANFAaIyenWo4fr1lMIqT4L-kS5qwXIpgq7Fsr6YMf9Jk130_assertion type Assertion NP583445.RANFAaIyenWo4fr1lMIqT4L-kS5qwXIpgq7Fsr6YMf9Jk130_head.
- NP583445.RANFAaIyenWo4fr1lMIqT4L-kS5qwXIpgq7Fsr6YMf9Jk130_assertion description "[The second phenotype, observed in four unrelated families, is autosomal dominant trismus-pseudocamptodactyly syndrome (distal arthrogryposis type 7; previously associated exclusively with myosin heavy chain 8 mutations).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP583445.RANFAaIyenWo4fr1lMIqT4L-kS5qwXIpgq7Fsr6YMf9Jk130_provenance.
- NP583445.RANFAaIyenWo4fr1lMIqT4L-kS5qwXIpgq7Fsr6YMf9Jk130_assertion evidence source_evidence_literature NP583445.RANFAaIyenWo4fr1lMIqT4L-kS5qwXIpgq7Fsr6YMf9Jk130_provenance.
- NP583445.RANFAaIyenWo4fr1lMIqT4L-kS5qwXIpgq7Fsr6YMf9Jk130_assertion SIO_000772 23413262 NP583445.RANFAaIyenWo4fr1lMIqT4L-kS5qwXIpgq7Fsr6YMf9Jk130_provenance.
- NP583445.RANFAaIyenWo4fr1lMIqT4L-kS5qwXIpgq7Fsr6YMf9Jk130_assertion wasDerivedFrom befree-20150227 NP583445.RANFAaIyenWo4fr1lMIqT4L-kS5qwXIpgq7Fsr6YMf9Jk130_provenance.
- NP583445.RANFAaIyenWo4fr1lMIqT4L-kS5qwXIpgq7Fsr6YMf9Jk130_assertion wasGeneratedBy ECO_0000203 NP583445.RANFAaIyenWo4fr1lMIqT4L-kS5qwXIpgq7Fsr6YMf9Jk130_provenance.