Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP589665.RA-aIEgi2AVxYrncQBur9VzHwTjmO5SPDZFfo9fVaFk_c130_assertion> ?p ?o ?g. }
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- NP589665.RA-aIEgi2AVxYrncQBur9VzHwTjmO5SPDZFfo9fVaFk_c130_assertion type Assertion NP589665.RA-aIEgi2AVxYrncQBur9VzHwTjmO5SPDZFfo9fVaFk_c130_head.
- NP589665.RA-aIEgi2AVxYrncQBur9VzHwTjmO5SPDZFfo9fVaFk_c130_assertion wasGeneratedBy ECO_0000203 NP589665.RA-aIEgi2AVxYrncQBur9VzHwTjmO5SPDZFfo9fVaFk_c130_provenance.
- NP589665.RA-aIEgi2AVxYrncQBur9VzHwTjmO5SPDZFfo9fVaFk_c130_assertion wasDerivedFrom befree-2016 NP589665.RA-aIEgi2AVxYrncQBur9VzHwTjmO5SPDZFfo9fVaFk_c130_provenance.
- NP589665.RA-aIEgi2AVxYrncQBur9VzHwTjmO5SPDZFfo9fVaFk_c130_assertion SIO_000772 17236141 NP589665.RA-aIEgi2AVxYrncQBur9VzHwTjmO5SPDZFfo9fVaFk_c130_provenance.
- NP589665.RA-aIEgi2AVxYrncQBur9VzHwTjmO5SPDZFfo9fVaFk_c130_assertion evidence source_evidence_literature NP589665.RA-aIEgi2AVxYrncQBur9VzHwTjmO5SPDZFfo9fVaFk_c130_provenance.
- NP589665.RA-aIEgi2AVxYrncQBur9VzHwTjmO5SPDZFfo9fVaFk_c130_assertion description "[Mutations in HOXD13 underlie syndactyly type V and a novel brachydactyly-syndactyly syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP589665.RA-aIEgi2AVxYrncQBur9VzHwTjmO5SPDZFfo9fVaFk_c130_provenance.