Matches in Nanopublications for { <http://rdf.disgenet.org/resource/nanopub/NP1327008.RAKVUalm0afpDGngCnaQsnF1R4fZ9BaXFweYx-E82MXCM130_assertion> ?p ?o ?g. }
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- NP1327008.RAKVUalm0afpDGngCnaQsnF1R4fZ9BaXFweYx-E82MXCM130_assertion type Assertion NP1327008.RAKVUalm0afpDGngCnaQsnF1R4fZ9BaXFweYx-E82MXCM130_head.
- NP1327008.RAKVUalm0afpDGngCnaQsnF1R4fZ9BaXFweYx-E82MXCM130_assertion description "[L1CAM, therefore, harbours mutations leading to either MASA syndrome or HSAS, and might be frequently implicated in X-linked mental retardation with or without hydrocephalus.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP1327008.RAKVUalm0afpDGngCnaQsnF1R4fZ9BaXFweYx-E82MXCM130_provenance.
- NP1327008.RAKVUalm0afpDGngCnaQsnF1R4fZ9BaXFweYx-E82MXCM130_assertion evidence source_evidence_literature NP1327008.RAKVUalm0afpDGngCnaQsnF1R4fZ9BaXFweYx-E82MXCM130_provenance.
- NP1327008.RAKVUalm0afpDGngCnaQsnF1R4fZ9BaXFweYx-E82MXCM130_assertion SIO_000772 7920660 NP1327008.RAKVUalm0afpDGngCnaQsnF1R4fZ9BaXFweYx-E82MXCM130_provenance.
- NP1327008.RAKVUalm0afpDGngCnaQsnF1R4fZ9BaXFweYx-E82MXCM130_assertion wasDerivedFrom befree-2016 NP1327008.RAKVUalm0afpDGngCnaQsnF1R4fZ9BaXFweYx-E82MXCM130_provenance.
- NP1327008.RAKVUalm0afpDGngCnaQsnF1R4fZ9BaXFweYx-E82MXCM130_assertion wasGeneratedBy ECO_0000203 NP1327008.RAKVUalm0afpDGngCnaQsnF1R4fZ9BaXFweYx-E82MXCM130_provenance.