Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP320034.RAIed6eHmVif_p8CqNfsGiCT9ZM2y2FtLN0Qdl0sk_9ek130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP320034.RAIed6eHmVif_p8CqNfsGiCT9ZM2y2FtLN0Qdl0sk_9ek130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP320034.RAIed6eHmVif_p8CqNfsGiCT9ZM2y2FtLN0Qdl0sk_9ek130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP320034.RAIed6eHmVif_p8CqNfsGiCT9ZM2y2FtLN0Qdl0sk_9ek130_provenance.
- NP320034.RAIed6eHmVif_p8CqNfsGiCT9ZM2y2FtLN0Qdl0sk_9ek130_assertion description "[Twenty-one unrelated children with persistent familial hematuria as well as their families were studied for segregation of hematuria with haplotypes at the COL4A3/COL4A4 locus for benign familial hematuria and at the COL4A5 locus for X-linked Alport syndrome.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP320034.RAIed6eHmVif_p8CqNfsGiCT9ZM2y2FtLN0Qdl0sk_9ek130_provenance.
- NP320034.RAIed6eHmVif_p8CqNfsGiCT9ZM2y2FtLN0Qdl0sk_9ek130_assertion evidence source_evidence_literature NP320034.RAIed6eHmVif_p8CqNfsGiCT9ZM2y2FtLN0Qdl0sk_9ek130_provenance.
- NP320034.RAIed6eHmVif_p8CqNfsGiCT9ZM2y2FtLN0Qdl0sk_9ek130_assertion SIO_000772 16235097 NP320034.RAIed6eHmVif_p8CqNfsGiCT9ZM2y2FtLN0Qdl0sk_9ek130_provenance.
- NP320034.RAIed6eHmVif_p8CqNfsGiCT9ZM2y2FtLN0Qdl0sk_9ek130_assertion wasDerivedFrom befree-20150227 NP320034.RAIed6eHmVif_p8CqNfsGiCT9ZM2y2FtLN0Qdl0sk_9ek130_provenance.
- NP320034.RAIed6eHmVif_p8CqNfsGiCT9ZM2y2FtLN0Qdl0sk_9ek130_assertion wasGeneratedBy ECO_0000203 NP320034.RAIed6eHmVif_p8CqNfsGiCT9ZM2y2FtLN0Qdl0sk_9ek130_provenance.
- befree-20150227 importedOn "2015-02-27" NP320034.RAIed6eHmVif_p8CqNfsGiCT9ZM2y2FtLN0Qdl0sk_9ek130_provenance.