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- NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_assertion type Assertion NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_head.
- NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_assertion wasGeneratedBy ECO_0000203 NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_provenance.
- NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_assertion wasDerivedFrom befree-20150227 NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_provenance.
- NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_assertion SIO_000772 21236492 NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_provenance.
- NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_assertion evidence source_evidence_literature NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_provenance.
- NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_assertion description "[A novel mutation of LAMB2 in a multigenerational mennonite family reveals a new phenotypic variant of Pierson syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP958138.RA9rcj5-paGOjhoK-WFBN7SQDpI-42tgkWrmKcWULBBkw130_provenance.