Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP195.RAuep4AOKlc_pMgznYDxvXuhuMFHUATyPoSnDeoFSEfbg130_assertion> ?p ?o ?g. }
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- NP195.RAuep4AOKlc_pMgznYDxvXuhuMFHUATyPoSnDeoFSEfbg130_assertion type Assertion NP195.RAuep4AOKlc_pMgznYDxvXuhuMFHUATyPoSnDeoFSEfbg130_head.
- NP195.RAuep4AOKlc_pMgznYDxvXuhuMFHUATyPoSnDeoFSEfbg130_assertion wasGeneratedBy ECO_0000218 NP195.RAuep4AOKlc_pMgznYDxvXuhuMFHUATyPoSnDeoFSEfbg130_provenance.
- NP195.RAuep4AOKlc_pMgznYDxvXuhuMFHUATyPoSnDeoFSEfbg130_assertion wasDerivedFrom uniprot-2016 NP195.RAuep4AOKlc_pMgznYDxvXuhuMFHUATyPoSnDeoFSEfbg130_provenance.
- NP195.RAuep4AOKlc_pMgznYDxvXuhuMFHUATyPoSnDeoFSEfbg130_assertion SIO_000772 10336779 NP195.RAuep4AOKlc_pMgznYDxvXuhuMFHUATyPoSnDeoFSEfbg130_provenance.
- NP195.RAuep4AOKlc_pMgznYDxvXuhuMFHUATyPoSnDeoFSEfbg130_assertion evidence source_evidence_curated NP195.RAuep4AOKlc_pMgznYDxvXuhuMFHUATyPoSnDeoFSEfbg130_provenance.
- NP195.RAuep4AOKlc_pMgznYDxvXuhuMFHUATyPoSnDeoFSEfbg130_assertion description "[Neurofibromatosis type 1 (NF1) is a dominant disorder caused by mutations in the NF1 gene; approximately 100 NF1 gene mutations have been published.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP195.RAuep4AOKlc_pMgznYDxvXuhuMFHUATyPoSnDeoFSEfbg130_provenance.