Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP453469.RAIdS_qVCSWxxi-sJp7pyegPXd2yRkydeMtYNVU2lltOk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP453469.RAIdS_qVCSWxxi-sJp7pyegPXd2yRkydeMtYNVU2lltOk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP453469.RAIdS_qVCSWxxi-sJp7pyegPXd2yRkydeMtYNVU2lltOk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP453469.RAIdS_qVCSWxxi-sJp7pyegPXd2yRkydeMtYNVU2lltOk130_provenance.
- NP453469.RAIdS_qVCSWxxi-sJp7pyegPXd2yRkydeMtYNVU2lltOk130_assertion description "[Crouzon syndrome: mutations in two spliceoforms of FGFR2 and a common point mutation shared with Jackson-Weiss syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP453469.RAIdS_qVCSWxxi-sJp7pyegPXd2yRkydeMtYNVU2lltOk130_provenance.
- NP453469.RAIdS_qVCSWxxi-sJp7pyegPXd2yRkydeMtYNVU2lltOk130_assertion evidence source_evidence_literature NP453469.RAIdS_qVCSWxxi-sJp7pyegPXd2yRkydeMtYNVU2lltOk130_provenance.
- NP453469.RAIdS_qVCSWxxi-sJp7pyegPXd2yRkydeMtYNVU2lltOk130_assertion SIO_000772 7581378 NP453469.RAIdS_qVCSWxxi-sJp7pyegPXd2yRkydeMtYNVU2lltOk130_provenance.
- NP453469.RAIdS_qVCSWxxi-sJp7pyegPXd2yRkydeMtYNVU2lltOk130_assertion wasDerivedFrom befree-20140225 NP453469.RAIdS_qVCSWxxi-sJp7pyegPXd2yRkydeMtYNVU2lltOk130_provenance.
- NP453469.RAIdS_qVCSWxxi-sJp7pyegPXd2yRkydeMtYNVU2lltOk130_assertion wasGeneratedBy ECO_0000203 NP453469.RAIdS_qVCSWxxi-sJp7pyegPXd2yRkydeMtYNVU2lltOk130_provenance.
- befree-20140225 importedOn "2014-02-25" NP453469.RAIdS_qVCSWxxi-sJp7pyegPXd2yRkydeMtYNVU2lltOk130_provenance.