Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP294324.RAwZnXobBMS2QCScSbQRfKrKCdabvq8h5Tzrj8rS1zvEw130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP294324.RAwZnXobBMS2QCScSbQRfKrKCdabvq8h5Tzrj8rS1zvEw130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP294324.RAwZnXobBMS2QCScSbQRfKrKCdabvq8h5Tzrj8rS1zvEw130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP294324.RAwZnXobBMS2QCScSbQRfKrKCdabvq8h5Tzrj8rS1zvEw130_provenance.
- NP294324.RAwZnXobBMS2QCScSbQRfKrKCdabvq8h5Tzrj8rS1zvEw130_assertion description "[The PMP22 gene is also involved in the majority of families with hereditary neuropathy with liability to pressure palsies (HNPP).]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP294324.RAwZnXobBMS2QCScSbQRfKrKCdabvq8h5Tzrj8rS1zvEw130_provenance.
- NP294324.RAwZnXobBMS2QCScSbQRfKrKCdabvq8h5Tzrj8rS1zvEw130_assertion evidence source_evidence_literature NP294324.RAwZnXobBMS2QCScSbQRfKrKCdabvq8h5Tzrj8rS1zvEw130_provenance.
- NP294324.RAwZnXobBMS2QCScSbQRfKrKCdabvq8h5Tzrj8rS1zvEw130_assertion SIO_000772 10975746 NP294324.RAwZnXobBMS2QCScSbQRfKrKCdabvq8h5Tzrj8rS1zvEw130_provenance.
- NP294324.RAwZnXobBMS2QCScSbQRfKrKCdabvq8h5Tzrj8rS1zvEw130_assertion wasDerivedFrom befree-2016 NP294324.RAwZnXobBMS2QCScSbQRfKrKCdabvq8h5Tzrj8rS1zvEw130_provenance.
- NP294324.RAwZnXobBMS2QCScSbQRfKrKCdabvq8h5Tzrj8rS1zvEw130_assertion wasGeneratedBy ECO_0000203 NP294324.RAwZnXobBMS2QCScSbQRfKrKCdabvq8h5Tzrj8rS1zvEw130_provenance.
- befree-2016 importedOn "2016-02-19" NP294324.RAwZnXobBMS2QCScSbQRfKrKCdabvq8h5Tzrj8rS1zvEw130_provenance.