Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP401125.RAodFpCtWU8IjSkz3EgHr9nm_uYFLuZF-t7txDLPWco8U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP401125.RAodFpCtWU8IjSkz3EgHr9nm_uYFLuZF-t7txDLPWco8U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP401125.RAodFpCtWU8IjSkz3EgHr9nm_uYFLuZF-t7txDLPWco8U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP401125.RAodFpCtWU8IjSkz3EgHr9nm_uYFLuZF-t7txDLPWco8U130_provenance.
- NP401125.RAodFpCtWU8IjSkz3EgHr9nm_uYFLuZF-t7txDLPWco8U130_assertion description "[Hypochondroplasia (HCH) is a skeletal dysplasia inherited in an autosomal dominant manner due, in most cases, to mutations in the fibroblast growth factor receptor 3 (FGFR3).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP401125.RAodFpCtWU8IjSkz3EgHr9nm_uYFLuZF-t7txDLPWco8U130_provenance.
- NP401125.RAodFpCtWU8IjSkz3EgHr9nm_uYFLuZF-t7txDLPWco8U130_assertion evidence source_evidence_literature NP401125.RAodFpCtWU8IjSkz3EgHr9nm_uYFLuZF-t7txDLPWco8U130_provenance.
- NP401125.RAodFpCtWU8IjSkz3EgHr9nm_uYFLuZF-t7txDLPWco8U130_assertion SIO_000772 18583390 NP401125.RAodFpCtWU8IjSkz3EgHr9nm_uYFLuZF-t7txDLPWco8U130_provenance.
- NP401125.RAodFpCtWU8IjSkz3EgHr9nm_uYFLuZF-t7txDLPWco8U130_assertion wasDerivedFrom befree-20150227 NP401125.RAodFpCtWU8IjSkz3EgHr9nm_uYFLuZF-t7txDLPWco8U130_provenance.
- NP401125.RAodFpCtWU8IjSkz3EgHr9nm_uYFLuZF-t7txDLPWco8U130_assertion wasGeneratedBy ECO_0000203 NP401125.RAodFpCtWU8IjSkz3EgHr9nm_uYFLuZF-t7txDLPWco8U130_provenance.
- befree-20150227 importedOn "2015-02-27" NP401125.RAodFpCtWU8IjSkz3EgHr9nm_uYFLuZF-t7txDLPWco8U130_provenance.