Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP729728.RAa8ZK4Gya8QLYYMkKYql71-SB998kfRRCgMygAOX48hg130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP729728.RAa8ZK4Gya8QLYYMkKYql71-SB998kfRRCgMygAOX48hg130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP729728.RAa8ZK4Gya8QLYYMkKYql71-SB998kfRRCgMygAOX48hg130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP729728.RAa8ZK4Gya8QLYYMkKYql71-SB998kfRRCgMygAOX48hg130_provenance.
- NP729728.RAa8ZK4Gya8QLYYMkKYql71-SB998kfRRCgMygAOX48hg130_assertion description "[Our findings expand the molecular, cellular, and clinical spectrum of HPS-2 and call for an increased index of suspicion for this diagnosis among patients with features of albinism, bleeding, and neutropenia.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP729728.RAa8ZK4Gya8QLYYMkKYql71-SB998kfRRCgMygAOX48hg130_provenance.
- NP729728.RAa8ZK4Gya8QLYYMkKYql71-SB998kfRRCgMygAOX48hg130_assertion evidence source_evidence_literature NP729728.RAa8ZK4Gya8QLYYMkKYql71-SB998kfRRCgMygAOX48hg130_provenance.
- NP729728.RAa8ZK4Gya8QLYYMkKYql71-SB998kfRRCgMygAOX48hg130_assertion SIO_000772 11809908 NP729728.RAa8ZK4Gya8QLYYMkKYql71-SB998kfRRCgMygAOX48hg130_provenance.
- NP729728.RAa8ZK4Gya8QLYYMkKYql71-SB998kfRRCgMygAOX48hg130_assertion wasDerivedFrom befree-20150227 NP729728.RAa8ZK4Gya8QLYYMkKYql71-SB998kfRRCgMygAOX48hg130_provenance.
- NP729728.RAa8ZK4Gya8QLYYMkKYql71-SB998kfRRCgMygAOX48hg130_assertion wasGeneratedBy ECO_0000203 NP729728.RAa8ZK4Gya8QLYYMkKYql71-SB998kfRRCgMygAOX48hg130_provenance.
- befree-20150227 importedOn "2015-02-27" NP729728.RAa8ZK4Gya8QLYYMkKYql71-SB998kfRRCgMygAOX48hg130_provenance.