Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP364218.RASicmleab8rPx0aMmWnSenx55B7ti6hrb8hYQ8TaNtAU130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP364218.RASicmleab8rPx0aMmWnSenx55B7ti6hrb8hYQ8TaNtAU130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP364218.RASicmleab8rPx0aMmWnSenx55B7ti6hrb8hYQ8TaNtAU130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP364218.RASicmleab8rPx0aMmWnSenx55B7ti6hrb8hYQ8TaNtAU130_provenance.
- NP364218.RASicmleab8rPx0aMmWnSenx55B7ti6hrb8hYQ8TaNtAU130_assertion description "[MYH11 mutations are rare and typically identified in patients with TAAD associated with PDA.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP364218.RASicmleab8rPx0aMmWnSenx55B7ti6hrb8hYQ8TaNtAU130_provenance.
- NP364218.RASicmleab8rPx0aMmWnSenx55B7ti6hrb8hYQ8TaNtAU130_assertion evidence source_evidence_literature NP364218.RASicmleab8rPx0aMmWnSenx55B7ti6hrb8hYQ8TaNtAU130_provenance.
- NP364218.RASicmleab8rPx0aMmWnSenx55B7ti6hrb8hYQ8TaNtAU130_assertion SIO_000772 21937134 NP364218.RASicmleab8rPx0aMmWnSenx55B7ti6hrb8hYQ8TaNtAU130_provenance.
- NP364218.RASicmleab8rPx0aMmWnSenx55B7ti6hrb8hYQ8TaNtAU130_assertion wasDerivedFrom befree-20140225 NP364218.RASicmleab8rPx0aMmWnSenx55B7ti6hrb8hYQ8TaNtAU130_provenance.
- NP364218.RASicmleab8rPx0aMmWnSenx55B7ti6hrb8hYQ8TaNtAU130_assertion wasGeneratedBy ECO_0000203 NP364218.RASicmleab8rPx0aMmWnSenx55B7ti6hrb8hYQ8TaNtAU130_provenance.
- befree-20140225 importedOn "2014-02-25" NP364218.RASicmleab8rPx0aMmWnSenx55B7ti6hrb8hYQ8TaNtAU130_provenance.