Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP8623.RAcvlT7_PQra1T9EIthPnCJN_bhcazhtTm2TonhEhTY5s130_assertion> ?p ?o ?g. }
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- NP8623.RAcvlT7_PQra1T9EIthPnCJN_bhcazhtTm2TonhEhTY5s130_assertion type Assertion NP8623.RAcvlT7_PQra1T9EIthPnCJN_bhcazhtTm2TonhEhTY5s130_head.
- NP8623.RAcvlT7_PQra1T9EIthPnCJN_bhcazhtTm2TonhEhTY5s130_assertion description "[X-linked spastic paraplegia (SPG1), MASA syndrome and X-linked hydrocephalus result from mutations in the L1 gene.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP8623.RAcvlT7_PQra1T9EIthPnCJN_bhcazhtTm2TonhEhTY5s130_provenance.
- NP8623.RAcvlT7_PQra1T9EIthPnCJN_bhcazhtTm2TonhEhTY5s130_assertion evidence source_evidence_curated NP8623.RAcvlT7_PQra1T9EIthPnCJN_bhcazhtTm2TonhEhTY5s130_provenance.
- NP8623.RAcvlT7_PQra1T9EIthPnCJN_bhcazhtTm2TonhEhTY5s130_assertion SIO_000772 7920659 NP8623.RAcvlT7_PQra1T9EIthPnCJN_bhcazhtTm2TonhEhTY5s130_provenance.
- NP8623.RAcvlT7_PQra1T9EIthPnCJN_bhcazhtTm2TonhEhTY5s130_assertion wasDerivedFrom uniprot-2016 NP8623.RAcvlT7_PQra1T9EIthPnCJN_bhcazhtTm2TonhEhTY5s130_provenance.
- NP8623.RAcvlT7_PQra1T9EIthPnCJN_bhcazhtTm2TonhEhTY5s130_assertion wasGeneratedBy ECO_0000218 NP8623.RAcvlT7_PQra1T9EIthPnCJN_bhcazhtTm2TonhEhTY5s130_provenance.