Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP241444.RAB4p6TvXuR0lspdp_kPv9nrD1opQiF2cT5HNNqPbbL7E130_assertion> ?p ?o ?g. }
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- NP241444.RAB4p6TvXuR0lspdp_kPv9nrD1opQiF2cT5HNNqPbbL7E130_assertion type Assertion NP241444.RAB4p6TvXuR0lspdp_kPv9nrD1opQiF2cT5HNNqPbbL7E130_head.
- NP241444.RAB4p6TvXuR0lspdp_kPv9nrD1opQiF2cT5HNNqPbbL7E130_assertion description "[In a patient with late-onset Alzheimer's disease, a novel allelic variant in exon 1 (g100169G > A) leads to p.Gly35Arg.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP241444.RAB4p6TvXuR0lspdp_kPv9nrD1opQiF2cT5HNNqPbbL7E130_provenance.
- NP241444.RAB4p6TvXuR0lspdp_kPv9nrD1opQiF2cT5HNNqPbbL7E130_assertion evidence source_evidence_literature NP241444.RAB4p6TvXuR0lspdp_kPv9nrD1opQiF2cT5HNNqPbbL7E130_provenance.
- NP241444.RAB4p6TvXuR0lspdp_kPv9nrD1opQiF2cT5HNNqPbbL7E130_assertion SIO_000772 18752597 NP241444.RAB4p6TvXuR0lspdp_kPv9nrD1opQiF2cT5HNNqPbbL7E130_provenance.
- NP241444.RAB4p6TvXuR0lspdp_kPv9nrD1opQiF2cT5HNNqPbbL7E130_assertion wasDerivedFrom lhgdn-20090331 NP241444.RAB4p6TvXuR0lspdp_kPv9nrD1opQiF2cT5HNNqPbbL7E130_provenance.
- NP241444.RAB4p6TvXuR0lspdp_kPv9nrD1opQiF2cT5HNNqPbbL7E130_assertion wasGeneratedBy ECO_0000203 NP241444.RAB4p6TvXuR0lspdp_kPv9nrD1opQiF2cT5HNNqPbbL7E130_provenance.