Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP324367.RAAHn_6bFtID_SKoJNLulgefLXVdpOBV23UXp1Ao0gSVw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP324367.RAAHn_6bFtID_SKoJNLulgefLXVdpOBV23UXp1Ao0gSVw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP324367.RAAHn_6bFtID_SKoJNLulgefLXVdpOBV23UXp1Ao0gSVw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP324367.RAAHn_6bFtID_SKoJNLulgefLXVdpOBV23UXp1Ao0gSVw130_provenance.
- NP324367.RAAHn_6bFtID_SKoJNLulgefLXVdpOBV23UXp1Ao0gSVw130_assertion description "[This is to our knowledge the first demonstration of a PAH missense variant with no apparent association to PAH deficiency.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP324367.RAAHn_6bFtID_SKoJNLulgefLXVdpOBV23UXp1Ao0gSVw130_provenance.
- NP324367.RAAHn_6bFtID_SKoJNLulgefLXVdpOBV23UXp1Ao0gSVw130_assertion evidence source_evidence_literature NP324367.RAAHn_6bFtID_SKoJNLulgefLXVdpOBV23UXp1Ao0gSVw130_provenance.
- NP324367.RAAHn_6bFtID_SKoJNLulgefLXVdpOBV23UXp1Ao0gSVw130_assertion SIO_000772 11461196 NP324367.RAAHn_6bFtID_SKoJNLulgefLXVdpOBV23UXp1Ao0gSVw130_provenance.
- NP324367.RAAHn_6bFtID_SKoJNLulgefLXVdpOBV23UXp1Ao0gSVw130_assertion wasDerivedFrom befree-2016 NP324367.RAAHn_6bFtID_SKoJNLulgefLXVdpOBV23UXp1Ao0gSVw130_provenance.
- NP324367.RAAHn_6bFtID_SKoJNLulgefLXVdpOBV23UXp1Ao0gSVw130_assertion wasGeneratedBy ECO_0000203 NP324367.RAAHn_6bFtID_SKoJNLulgefLXVdpOBV23UXp1Ao0gSVw130_provenance.
- befree-2016 importedOn "2016-02-19" NP324367.RAAHn_6bFtID_SKoJNLulgefLXVdpOBV23UXp1Ao0gSVw130_provenance.