Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_provenance.
- NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_assertion description "[Classic and atypical fibrodysplasia ossificans progressiva (FOP) phenotypes are caused by mutations in the bone morphogenetic protein (BMP) type I receptor ACVR1.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_provenance.
- NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_assertion evidence source_evidence_literature NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_provenance.
- NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_assertion SIO_000772 19085907 NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_provenance.
- NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_assertion wasDerivedFrom befree-2016 NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_provenance.
- NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_assertion wasGeneratedBy ECO_0000203 NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_provenance.
- befree-2016 importedOn "2016-02-19" NP709502.RAaJyGjjINEDxE5lQi7NEtYoPBH1SeCwkD3x1qzalst0o130_provenance.