Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP587848.RAVatnXTd2GKoHvo4QWRglMBvvtZG3Jv7RnL4HVZLGjDU130_assertion> ?p ?o ?g. }
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- NP587848.RAVatnXTd2GKoHvo4QWRglMBvvtZG3Jv7RnL4HVZLGjDU130_assertion type Assertion NP587848.RAVatnXTd2GKoHvo4QWRglMBvvtZG3Jv7RnL4HVZLGjDU130_head.
- NP587848.RAVatnXTd2GKoHvo4QWRglMBvvtZG3Jv7RnL4HVZLGjDU130_assertion wasGeneratedBy ECO_0000203 NP587848.RAVatnXTd2GKoHvo4QWRglMBvvtZG3Jv7RnL4HVZLGjDU130_provenance.
- NP587848.RAVatnXTd2GKoHvo4QWRglMBvvtZG3Jv7RnL4HVZLGjDU130_assertion wasDerivedFrom befree-20150227 NP587848.RAVatnXTd2GKoHvo4QWRglMBvvtZG3Jv7RnL4HVZLGjDU130_provenance.
- NP587848.RAVatnXTd2GKoHvo4QWRglMBvvtZG3Jv7RnL4HVZLGjDU130_assertion SIO_000772 15735646 NP587848.RAVatnXTd2GKoHvo4QWRglMBvvtZG3Jv7RnL4HVZLGjDU130_provenance.
- NP587848.RAVatnXTd2GKoHvo4QWRglMBvvtZG3Jv7RnL4HVZLGjDU130_assertion evidence source_evidence_literature NP587848.RAVatnXTd2GKoHvo4QWRglMBvvtZG3Jv7RnL4HVZLGjDU130_provenance.
- NP587848.RAVatnXTd2GKoHvo4QWRglMBvvtZG3Jv7RnL4HVZLGjDU130_assertion description "[Autosomal dominant mutations in the gene encoding the basic helix-loop-helix transcription factor Twist1 are associated with limb and craniofacial defects in humans with Saethre-Chotzen syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP587848.RAVatnXTd2GKoHvo4QWRglMBvvtZG3Jv7RnL4HVZLGjDU130_provenance.