Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1364609.RAKqtPTpdLkLAHPoAyiwyyYBgCJLU2nkMS5eWqpNGc_As130_assertion> ?p ?o ?g. }
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- NP1364609.RAKqtPTpdLkLAHPoAyiwyyYBgCJLU2nkMS5eWqpNGc_As130_assertion type Assertion NP1364609.RAKqtPTpdLkLAHPoAyiwyyYBgCJLU2nkMS5eWqpNGc_As130_head.
- NP1364609.RAKqtPTpdLkLAHPoAyiwyyYBgCJLU2nkMS5eWqpNGc_As130_assertion wasGeneratedBy ECO_0000203 NP1364609.RAKqtPTpdLkLAHPoAyiwyyYBgCJLU2nkMS5eWqpNGc_As130_provenance.
- NP1364609.RAKqtPTpdLkLAHPoAyiwyyYBgCJLU2nkMS5eWqpNGc_As130_assertion wasDerivedFrom befree-2016 NP1364609.RAKqtPTpdLkLAHPoAyiwyyYBgCJLU2nkMS5eWqpNGc_As130_provenance.
- NP1364609.RAKqtPTpdLkLAHPoAyiwyyYBgCJLU2nkMS5eWqpNGc_As130_assertion SIO_000772 8972002 NP1364609.RAKqtPTpdLkLAHPoAyiwyyYBgCJLU2nkMS5eWqpNGc_As130_provenance.
- NP1364609.RAKqtPTpdLkLAHPoAyiwyyYBgCJLU2nkMS5eWqpNGc_As130_assertion evidence source_evidence_literature NP1364609.RAKqtPTpdLkLAHPoAyiwyyYBgCJLU2nkMS5eWqpNGc_As130_provenance.
- NP1364609.RAKqtPTpdLkLAHPoAyiwyyYBgCJLU2nkMS5eWqpNGc_As130_assertion description "[Gene mutations in 21 unrelated cases of phenotypic heterozygous protein C deficiency and thrombosis. Protein C Study Group.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1364609.RAKqtPTpdLkLAHPoAyiwyyYBgCJLU2nkMS5eWqpNGc_As130_provenance.