Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/nanopublications.trig#NP723685.RA-321R40j7Kwr2MPO50ub0lXTgsCxQ4CoHkZuGt5pLm0130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP723685.RA-321R40j7Kwr2MPO50ub0lXTgsCxQ4CoHkZuGt5pLm0130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP723685.RA-321R40j7Kwr2MPO50ub0lXTgsCxQ4CoHkZuGt5pLm0130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP723685.RA-321R40j7Kwr2MPO50ub0lXTgsCxQ4CoHkZuGt5pLm0130_provenance.
- NP723685.RA-321R40j7Kwr2MPO50ub0lXTgsCxQ4CoHkZuGt5pLm0130_assertion description "[Frontometaphyseal dysplasia (FMD) belongs to a group of overlapping skeletal dysplasias, the common molecular basis of which are mutations of FLNA, the gene encoding filamin A.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP723685.RA-321R40j7Kwr2MPO50ub0lXTgsCxQ4CoHkZuGt5pLm0130_provenance.
- NP723685.RA-321R40j7Kwr2MPO50ub0lXTgsCxQ4CoHkZuGt5pLm0130_assertion evidence source_evidence_literature NP723685.RA-321R40j7Kwr2MPO50ub0lXTgsCxQ4CoHkZuGt5pLm0130_provenance.
- NP723685.RA-321R40j7Kwr2MPO50ub0lXTgsCxQ4CoHkZuGt5pLm0130_assertion SIO_000772 16596676 NP723685.RA-321R40j7Kwr2MPO50ub0lXTgsCxQ4CoHkZuGt5pLm0130_provenance.
- NP723685.RA-321R40j7Kwr2MPO50ub0lXTgsCxQ4CoHkZuGt5pLm0130_assertion wasDerivedFrom befree-20140225 NP723685.RA-321R40j7Kwr2MPO50ub0lXTgsCxQ4CoHkZuGt5pLm0130_provenance.
- NP723685.RA-321R40j7Kwr2MPO50ub0lXTgsCxQ4CoHkZuGt5pLm0130_assertion wasGeneratedBy ECO_0000203 NP723685.RA-321R40j7Kwr2MPO50ub0lXTgsCxQ4CoHkZuGt5pLm0130_provenance.
- befree-20140225 importedOn "2014-02-25" NP723685.RA-321R40j7Kwr2MPO50ub0lXTgsCxQ4CoHkZuGt5pLm0130_provenance.