Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance.
- NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_assertion wasGeneratedBy ECO_0000203 NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance.
- NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_assertion wasDerivedFrom befree-20140225 NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance.
- NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_assertion SIO_000772 19785597 NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance.
- NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_assertion evidence source_evidence_literature NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance.
- NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_assertion description "[Pachyonychia congenita (PC), a rare autosomal-dominant keratin disorder caused by mutations in keratin genes KRT6A/B, KRT16 or KRT17, is characterized by painful plantar keratoderma and hypertrophic nail dystrophy.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance.
- befree-20140225 importedOn "2014-02-25" NP311847.RAkemUO7kXxnTsOui0FbTcD1CtERRBsiUfbm6W3vgqypA130_provenance.