Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP6332.RAns1mPHUTNQDiNBMWOtj8F9lWgIvCax4bWtP58aU6W-k130_provenance>. }
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- source_evidence_curated type ECO_0000205 NP6332.RAns1mPHUTNQDiNBMWOtj8F9lWgIvCax4bWtP58aU6W-k130_provenance.
- source_evidence_curated label "DisGeNET evidence - CURATED" NP6332.RAns1mPHUTNQDiNBMWOtj8F9lWgIvCax4bWtP58aU6W-k130_provenance.
- source_evidence_curated comment "Gene-disease associations manually curated." NP6332.RAns1mPHUTNQDiNBMWOtj8F9lWgIvCax4bWtP58aU6W-k130_provenance.
- NP6332.RAns1mPHUTNQDiNBMWOtj8F9lWgIvCax4bWtP58aU6W-k130_assertion description "[De novo ACTA2 mutation causes a novel syndrome of multisystemic smooth muscle dysfunction.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP6332.RAns1mPHUTNQDiNBMWOtj8F9lWgIvCax4bWtP58aU6W-k130_provenance.
- NP6332.RAns1mPHUTNQDiNBMWOtj8F9lWgIvCax4bWtP58aU6W-k130_assertion evidence source_evidence_curated NP6332.RAns1mPHUTNQDiNBMWOtj8F9lWgIvCax4bWtP58aU6W-k130_provenance.
- NP6332.RAns1mPHUTNQDiNBMWOtj8F9lWgIvCax4bWtP58aU6W-k130_assertion SIO_000772 20734336 NP6332.RAns1mPHUTNQDiNBMWOtj8F9lWgIvCax4bWtP58aU6W-k130_provenance.
- NP6332.RAns1mPHUTNQDiNBMWOtj8F9lWgIvCax4bWtP58aU6W-k130_assertion wasDerivedFrom uniprot-2016 NP6332.RAns1mPHUTNQDiNBMWOtj8F9lWgIvCax4bWtP58aU6W-k130_provenance.
- NP6332.RAns1mPHUTNQDiNBMWOtj8F9lWgIvCax4bWtP58aU6W-k130_assertion wasGeneratedBy ECO_0000218 NP6332.RAns1mPHUTNQDiNBMWOtj8F9lWgIvCax4bWtP58aU6W-k130_provenance.
- uniprot-2016 importedOn "2016-01-25" NP6332.RAns1mPHUTNQDiNBMWOtj8F9lWgIvCax4bWtP58aU6W-k130_provenance.